A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964906



Internal ID18600142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:94563640..94574067hg38UCSC Ensembl
Innerchr5:93899345..93909772hg19UCSC Ensembl
Innerchr5:93925101..93935528hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3810428
hg1910428
hg1810428
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2368755, nssv2368751, nssv2368753, nssv2368757, nssv2368750, nssv2368749, nssv2368758, nssv2368754, nssv2368752, nssv2368756
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesKIAA0825
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964906
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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