A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965225



Internal ID18600459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:156040407..156049287hg38UCSC Ensembl
Innerchr3:155758196..155767076hg19UCSC Ensembl
Innerchr3:157240890..157249770hg18UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg388881
hg198881
hg188881
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2301819, nssv2301822, nssv2301825, nssv2301817, nssv2301820, nssv2301818, nssv2301823, nssv2301824, nssv2301821, nssv2301826
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)nsv965225
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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