A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000081



Internal ID18742612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:57698749..57926706hg38UCSC Ensembl
Innerchr3:57684476..57912433hg19UCSC Ensembl
Innerchr3:57659516..57887473hg18UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38227958
hg19227958
hg18227958
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593387
Samples
Known GenesSLMAP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1000081
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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