A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960087



Internal ID18595340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:31009047..31022674hg38UCSC Ensembl
Innerchr17:29336065..29349692hg19UCSC Ensembl
Innerchr17:26360191..26373818hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3813628
hg1913628
hg1813628
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2090317, nssv2090312, nssv2090313, nssv2090310, nssv2090308, nssv2090315, nssv2090311, nssv2090309, nssv2090314, nssv2090316
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)nsv960087
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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