A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968612



Internal ID18603840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:35962966..35980516hg38UCSC Ensembl
Innerchr9:35962963..35980513hg19UCSC Ensembl
Innerchr9:35952963..35970513hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3817551
hg1917551
hg1817551
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2526827, nssv2526819, nssv2526824, nssv2526820, nssv2526828, nssv2526823, nssv2526825, nssv2526822, nssv2526826, nssv2526821
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)nsv968612
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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