A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980265



Internal ID18615465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:146523247..146533792hg38UCSC Ensembl
Innerchr4:147444399..147454944hg19UCSC Ensembl
Innerchr4:147663849..147674394hg18UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg3810546
hg1910546
hg1810546
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2337393, nssv2337395, nssv2337392, nssv2337391, nssv2337397, nssv2337394, nssv2337398, nssv2337389, nssv2337396, nssv2337390
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)nsv980265
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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