A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960423



Internal ID18248988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:16186551..16209359hg38UCSC Ensembl
Innerchr17:16089865..16112673hg19UCSC Ensembl
Innerchr17:16030590..16053398hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3822809
hg1922809
hg1822809
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2079123, nssv2079130, nssv2079128, nssv2079124, nssv2079126, nssv2079131, nssv2079125, nssv2079132, nssv2079129, nssv2079127
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesNCOR1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960423
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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