A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962263



Internal ID18597507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15808917..15813444hg38UCSC Ensembl
Innerchr17:15712231..15716758hg19UCSC Ensembl
Innerchr17:15652956..15657483hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg384528
hg194528
hg184528
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2078967, nssv2078970, nssv2078973, nssv2078972, nssv2078965, nssv2078969, nssv2078968, nssv2078966, nssv2078964, nssv2078971
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)nsv962263
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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