A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960077



Internal ID18595330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:20814587..20819407hg38UCSC Ensembl
Innerchr17:20717900..20722720hg19UCSC Ensembl
Innerchr17:20658492..20663312hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg384821
hg194821
hg184821
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2084893, nssv2084890, nssv2084885, nssv2084891, nssv2084892, nssv2084894, nssv2084889, nssv2084888, nssv2084886, nssv2084887
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)nsv960077
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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