A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2716597



Internal ID10300233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:83031813..83032722hg38UCSC Ensembl
Outerchr17:80989689..80990598hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38910
hg19910
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6703242, essv6717581, essv6729051, essv6678575, essv6913370, essv6682291, essv6971632, essv6843242, essv6835597, essv6772843, essv6941164, essv6916842, essv6905614, essv6796824, essv6674368, essv6706890, essv6725246, essv6713671, essv6801040, essv6780217, essv6788549
SamplesSSM071, SSM045, SSM046, SSM065, SSM039, SSM013, SSM042, SSM028, SSM084, SSM069, SSM032, SSM031, SSM067, SSM033, SSM040, SSM072, SSM082, SSM015, SSM016, SSM022, SSM043
Known GenesB3GNTL1
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)esv2716597
Frequency
Sample Size96
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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