A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2735595



Internal ID9969926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:37505935..37506232hg38UCSC Ensembl
Outerchr10:37794863..37795160hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6838319, essv6783219, essv6850674, essv6716463, essv6965255, essv6842136, essv6809136, essv6827379, essv6806139
SamplesSSM083, SSM027, SSM075, SSM074, SSM084, SSM086, SSM068, SSM080, SSM043
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)esv2735595
Frequency
Sample Size96
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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