A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974592



Internal ID18609803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:66994172..67001073hg38UCSC Ensembl
Innerchr15:67286510..67293411hg19UCSC Ensembl
Innerchr15:65073564..65080465hg18UCSC Ensembl
Cytoband15q22.32
Allele length
AssemblyAllele length
hg386902
hg196902
hg186902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2028808, nssv2028812, nssv2028810, nssv2028809, nssv2028807, nssv2028813, nssv2028804, nssv2028811, nssv2028805, nssv2028806
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)nsv974592
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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