A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2740657



Internal ID10324293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:11680497..11683299hg38UCSC Ensembl
OuterchrY:13801203..13804005hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg382803
hg192803
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1333e201
Supporting Variantsessv6917033, essv6820792, essv6921252, essv6696600, essv6871407, essv6967352, essv6780621, essv6780427, essv6756259, essv6946930, essv6696601, essv6744663, essv6843444, essv6917034, essv6835795, essv6747503, essv6780632, essv6946918, essv6925275, essv6888719
SamplesSSM008, SSM027, SSM058, SSM084, SSM090, SSM018, SSM096, SSM017, SSM003, SSM067, SSM082, SSM078, SSM016, SSM053, SSM037, SSM055
Known Genes
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)esv2740657
Frequency
Sample Size96
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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