A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965897



Internal ID18601127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64280475..64292795hg38UCSC Ensembl
Innerchr20:62911828..62924148hg19UCSC Ensembl
Innerchr20:62382272..62394592hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3812321
hg1912321
hg1812321
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2241614, nssv2241619, nssv2241615, nssv2241617, nssv2241616, nssv2241611, nssv2241613, nssv2241620, nssv2241618, nssv2241612
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLINC00266-1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965897
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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