A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976963



Internal ID18612169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90271318..90301397hg38UCSC Ensembl
Innerchr15:90814550..90844629hg19UCSC Ensembl
Innerchr15:88615554..88645633hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3830080
hg1930080
hg1830080
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2038406, nssv2038402, nssv2038403, nssv2038399, nssv2038401, nssv2038398, nssv2038400, nssv2038405, nssv2038407, nssv2038404
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesNGRN
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976963
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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