A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963347



Internal ID18598588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:101599277..101624054hg38UCSC Ensembl
Innerchr3:101318121..101342898hg19UCSC Ensembl
Innerchr3:102800811..102825588hg18UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg3824778
hg1924778
hg1824778
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2292104, nssv2292103, nssv2292107, nssv2292101, nssv2292106, nssv2292102, nssv2292100, nssv2292099, nssv2292098, nssv2292105
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)nsv963347
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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