A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965982



Internal ID18601212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33410869..33413190hg38UCSC Ensembl
Innerchr21:34783175..34785496hg19UCSC Ensembl
Innerchr21:33705045..33707366hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg382322
hg192322
hg182322
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2247427, nssv2247428, nssv2247431, nssv2247429, nssv2247423, nssv2247432, nssv2247426, nssv2247430, nssv2247425, nssv2247424
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesIFNGR2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965982
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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