A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977718



Internal ID18612924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:56323190..56325690hg38UCSC Ensembl
Innerchr15:56615388..56617888hg19UCSC Ensembl
Innerchr15:54402680..54405180hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg382501
hg192501
hg182501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2025712, nssv2025716, nssv2025713, nssv2025708, nssv2025715, nssv2025709, nssv2025714, nssv2025717, nssv2025711, nssv2025710
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)nsv977718
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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