A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967733



Internal ID18602961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:22594160..22610052hg38UCSC Ensembl
Innerchr4:22595783..22611675hg19UCSC Ensembl
Innerchr4:22204881..22220773hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3815893
hg1915893
hg1815893
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2313392, nssv2313396, nssv2313394, nssv2313395, nssv2313400, nssv2313397, nssv2313398, nssv2313393, nssv2313399, nssv2313401
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)nsv967733
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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