A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979900



Internal ID18615101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:169903110..169905815hg38UCSC Ensembl
Innerchr3:169620898..169623603hg19UCSC Ensembl
Innerchr3:171103592..171106297hg18UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg382706
hg192706
hg182706
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2305405, nssv2305402, nssv2305410, nssv2305403, nssv2305401, nssv2305404, nssv2305407, nssv2305409, nssv2305408, nssv2305406
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)nsv979900
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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