A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964384



Internal ID18599622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:25615913..25616413hg38UCSC Ensembl
Innerchr20:25596549..25597049hg19UCSC Ensembl
Innerchr20:25544549..25545049hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2232197, nssv2232196, nssv2232202, nssv2232200, nssv2232194, nssv2232199, nssv2232203, nssv2232198, nssv2232195, nssv2232201
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesNANP
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964384
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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