A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982357



Internal ID18617552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28655..32355hg38UCSC Ensembl
Innerchr9:28655..32355hg19UCSC Ensembl
Innerchr9:18655..22355hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg383701
hg193701
hg183701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2724433, nssv2724434, nssv2724436, nssv2724430, nssv2724437, nssv2724435, nssv2724432, nssv2724431, nssv2724438, nssv2724439
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesWASH1
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982357
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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