A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967731



Internal ID18602959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:20031656..20037795hg38UCSC Ensembl
Innerchr4:20033279..20039418hg19UCSC Ensembl
Innerchr4:19642377..19648516hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg386140
hg196140
hg186140
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2312941, nssv2312936, nssv2312937, nssv2312934, nssv2312942, nssv2312940, nssv2312943, nssv2312935, nssv2312939, nssv2312938
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)nsv967731
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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