A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052761



Internal ID19141980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6977644..7009688hg38UCSC Ensembl
Innerchr10:7019606..7051650hg19UCSC Ensembl
Innerchr10:7059612..7091656hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3832045
hg1932045
hg1832045
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3494073
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)nsv1052761
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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