A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962328



Internal ID18597572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:43224816..43310704hg38UCSC Ensembl
Innerchr17:41376839..41388059hg19UCSC Ensembl
Innerchr17:38732365..38743585hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3885889
hg1911221
hg1811221
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2097717, nssv2097724, nssv2097723, nssv2097720, nssv2097718, nssv2097725, nssv2097721, nssv2097719, nssv2097726, nssv2097722
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLINC00854
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv962328
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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