A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042462



Internal ID19131681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:55294078..55401629hg38UCSC Ensembl
Innerchr13:55868213..55975764hg19UCSC Ensembl
Innerchr13:54766214..54873765hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38107552
hg19107552
hg18107552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1657n100
Supporting Variantsnssv3523864
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)nsv1042462
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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