A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962271



Internal ID18597515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:17008950..17019532hg38UCSC Ensembl
Innerchr17:16912264..16922846hg19UCSC Ensembl
Innerchr17:16852989..16863571hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3810583
hg1910583
hg1810583
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2081880, nssv2081873, nssv2081878, nssv2081877, nssv2081872, nssv2081871, nssv2081875, nssv2081879, nssv2081874, nssv2081876
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)nsv962271
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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