A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2737204



Internal ID9971540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:76644379..76645822hg38UCSC Ensembl
Outerchr8:77556614..77558057hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg381444
hg191444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6805929, essv6915634, essv6737450, essv6716181, essv6845490, essv6685042, essv6884696, essv6766632, essv6970118, essv6763010, essv6818972, essv6731519, essv6894110, essv6814915, essv6897210, essv6944220, essv6861637, essv6705673, essv6760546, essv6803059, essv6771469, essv6782910, essv6958178, essv6765425, essv6801088, essv6935433, essv6830686, essv6768045, essv6698351, essv6778856, essv6838050, essv6952604, essv6927404, essv6976000, essv6893721, essv6740544, essv6966572, essv6681034, essv6919547, essv6911988, essv6775169, essv6707610, essv6712466, essv6931170, essv6755064, essv6850207, essv6691082, essv6873261, essv6934041, essv6746400, essv6787118, essv6823032, essv6964782, essv6939699, essv6904361, essv6727752, essv6791220, essv6672138, essv6887534, essv6881895, essv6834374, essv6752118, essv6811793, essv6830763, essv6683454, essv6723908, essv6923689, essv6795379, essv6733832, essv6870295, essv6841874, essv6720097, essv6900186, essv6904819, essv6708993, essv6757851, essv6749237, essv6879071, essv6856234, essv6948448, essv6694886
SamplesSSM010, SSM065, SSM022, SSM007, SSM027, SSM013, SSM082, SSM086, SSM006, SSM036, SSM055, SSM091, SSM033, SSM084, SSM061, SSM099, SSM042, SSM040, SSM078, SSM043, SSM088, SSM090, SSM064, SSM031, SSM025, SSM020, SSM071, SSM016, SSM057, SSM001, SSM024, SSM045, SSM067, SSM094, SSM083, SSM050, SSM041, SSM077, SSM062, SSM005, SSM012, SSM093, SSM100, SSM056, SSM085, SSM017, SSM009, SSM066, SSM028, SSM029, SSM003, SSM095, SSM047, SSM073, SSM069, SSM021, SSM002, SSM037, SSM063, SSM087, SSM038, SSM046, SSM019, SSM096, SSM023, SSM079, SSM052, SSM068, SSM044, SSM074, SSM004, SSM015, SSM026, SSM008, SSM098, SSM018, SSM076, SSM058, SSM059, SSM081, SSM070
Known GenesZFHX4-AS1
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)esv2737204
Frequency
Sample Size96
Observed Gain0
Observed Loss81
Observed Complex0
Frequencyn/a


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