A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976931



Internal ID18612137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:46341252..46341898hg38UCSC Ensembl
Innerchr15:46633450..46634096hg19UCSC Ensembl
Innerchr15:44420742..44421388hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38647
hg19647
hg18647
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2023131, nssv2023138, nssv2023137, nssv2023134, nssv2023135, nssv2023132, nssv2023140, nssv2023133, nssv2023139, nssv2023136
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976931
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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