A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2744651



Internal ID10325621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:67706963..67990016hg38UCSC Ensembl
Outerchr11:67474434..67757487hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38283054
hg19283054
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6749593, essv6907884, essv6760883, essv6740964, essv6716681, essv6959091, essv6771955, essv6770932, essv6857028, essv6712884, essv6812137, essv6970676, essv6959092, essv6672970, essv6823530, essv6879405, essv6755453, essv6752489, essv6891170, essv6850999, essv6755452, essv6827600, essv6749594, essv6965611, essv6907895, essv6827597, essv6815366, essv6876564, essv6806288, essv6688195, essv6970340, essv6900557, essv6803412, essv6916026
SamplesSSM100, SSM008, SSM027, SSM079, SSM065, SSM087, SSM097, SSM073, SSM093, SSM074, SSM042, SSM002, SSM057, SSM058, SSM028, SSM092, SSM061, SSM026, SSM035, SSM031, SSM086, SSM016, SSM080, SSM077, SSM076, SSM004, SSM043, SSM052, SSM056
Known GenesFAM86C2P
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)esv2744651
Frequency
Sample Size96
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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