A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053615



Internal ID19142834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:37491853..37510608hg38UCSC Ensembl
Innerchr13:38065990..38084745hg19UCSC Ensembl
Innerchr13:36963990..36982745hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3818756
hg1918756
hg1818756
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1627n100
Supporting Variantsnssv3523251, nssv3523249, nssv3523250
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)nsv1053615
Frequency
Sample Size11257
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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