A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980189



Internal ID18615389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:33823013..33825492hg38UCSC Ensembl
Innerchr4:33824635..33827114hg19UCSC Ensembl
Innerchr4:33501030..33503509hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg382480
hg192480
hg182480
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2313851, nssv2313855, nssv2313856, nssv2313850, nssv2313854, nssv2313852, nssv2313849, nssv2313853, nssv2313847, nssv2313848
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)nsv980189
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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