A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972659



Internal ID18607875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:32332917..32334184hg38UCSC Ensembl
Innerchr9:32332915..32334182hg19UCSC Ensembl
Innerchr9:32322915..32324182hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg381268
hg191268
hg181268
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2526147, nssv2526138, nssv2526140, nssv2526144, nssv2526139, nssv2526142, nssv2526146, nssv2526145, nssv2526141, nssv2526143
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)nsv972659
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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