A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976939



Internal ID18612145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57976104..57980105hg38UCSC Ensembl
Innerchr15:58268302..58272303hg19UCSC Ensembl
Innerchr15:56055594..56059595hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg384002
hg194002
hg184002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2026260, nssv2026255, nssv2026263, nssv2026256, nssv2026258, nssv2026262, nssv2026257, nssv2026261, nssv2026254, nssv2026259
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesALDH1A2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976939
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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