A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976937



Internal ID18612143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:55190767..55191267hg38UCSC Ensembl
Innerchr15:55482965..55483465hg19UCSC Ensembl
Innerchr15:53270257..53270757hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2025602, nssv2025601, nssv2025598, nssv2025597, nssv2025603, nssv2025596, nssv2025604, nssv2025599, nssv2025600, nssv2025605
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRSL24D1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976937
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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