A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972299



Internal ID18260829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21141265..21142529hg38UCSC Ensembl
Innerchr9:21141264..21142528hg19UCSC Ensembl
Innerchr9:21131264..21132528hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg381265
hg191265
hg181265
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2524246, nssv2524245, nssv2524243, nssv2524249, nssv2524244, nssv2524241, nssv2524247, nssv2524248, nssv2524242, nssv2524250
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesIFNW1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972299
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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