A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3707755



Internal ID19006036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:36883876..37107580hg38UCSC Ensembl
Innerchr10:37172804..37396508hg19UCSC Ensembl
Innerchr10:37212810..37436514hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38223705
hg19223705
hg18223705
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036571
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3707755
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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