A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969660



Internal ID18604887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67913212..67919820hg38UCSC Ensembl
Innerchr9:67980658..67987266hg19UCSC Ensembl
Innerchr9:67570478..67577086hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg386609
hg196609
hg186609
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv92n82
Supporting Variantsnssv2742646, nssv2742644, nssv2742642, nssv2742648, nssv2742643, nssv2742641, nssv2742645, nssv2742640, nssv2742647, nssv2742649
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969660
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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