A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964113



Internal ID18599351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:169744158..169746020hg38UCSC Ensembl
Innerchr4:170665309..170667171hg19UCSC Ensembl
Innerchr4:170901884..170903746hg18UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg381863
hg191863
hg181863
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2342480, nssv2342485, nssv2342477, nssv2342482, nssv2342483, nssv2342484, nssv2342478, nssv2342481, nssv2342486, nssv2342479
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesC4orf27
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964113
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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