A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2729585



Internal ID9963900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1213736..1214622hg38UCSC Ensembl
Outerchr10:1259676..1260562hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38887
hg19887
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6712675, essv6830956, essv6768520, essv6842080, essv6882049, essv6876381, essv6944492, essv6795646, essv6771700, essv6919768, essv6970383, essv6716394, essv6743751, essv6832177, essv6952831, essv6834564, essv6976426, essv6802854, essv6768215, essv6727967, essv6931430, essv6904563, essv6684766, essv6731740, essv6827321, essv6850574
SamplesSSM010, SSM065, SSM092, SSM013, SSM053, SSM082, SSM086, SSM084, SSM042, SSM043, SSM064, SSM025, SSM020, SSM071, SSM094, SSM017, SSM009, SSM028, SSM029, SSM047, SSM034, SSM046, SSM023, SSM008, SSM081, SSM080
Known GenesADARB2
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)esv2729585
Frequency
Sample Size96
Observed Gain0
Observed Loss26
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer