A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001910



Internal ID18744441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46760315..46790579hg38UCSC Ensembl
Innerchr3:46801805..46832069hg19UCSC Ensembl
Innerchr3:46776809..46807073hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3830265
hg1930265
hg1830265
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4735n100
Supporting Variantsnssv3591042, nssv3591039, nssv3591040, nssv3591038, nssv3591041
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)nsv1001910
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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