A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974583



Internal ID18263108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58686811..58695251hg38UCSC Ensembl
Innerchr15:58979010..58987450hg19UCSC Ensembl
Innerchr15:56766302..56774742hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg388441
hg198441
hg188441
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2026569, nssv2026574, nssv2026571, nssv2026567, nssv2026575, nssv2026570, nssv2026573, nssv2026568, nssv2026572, nssv2026566
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesADAM10, HSP90AB4P
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974583
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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