A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962362



Internal ID18597606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:67271675..67272589hg38UCSC Ensembl
Innerchr17:65267791..65268705hg19UCSC Ensembl
Innerchr17:62698253..62699167hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38915
hg19915
hg18915
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2108640, nssv2108634, nssv2108637, nssv2108631, nssv2108633, nssv2108639, nssv2108636, nssv2108638, nssv2108632, nssv2108635
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)nsv962362
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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