A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967727



Internal ID18602955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15766585..15769060hg38UCSC Ensembl
Innerchr4:15768208..15770683hg19UCSC Ensembl
Innerchr4:15377306..15379781hg18UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg382476
hg192476
hg182476
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2314488, nssv2314491, nssv2314489, nssv2314490, nssv2314487, nssv2314492, nssv2314493, nssv2314496, nssv2314494, nssv2314495
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)nsv967727
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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