A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010901



Internal ID19100118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:146932256..147188716hg38UCSC Ensembl
Innerchr3:146650043..146906503hg19UCSC Ensembl
Innerchr3:148132733..148389193hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38256461
hg19256461
hg18256461
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3606166
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)nsv1010901
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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