A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971643



Internal ID18606860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:37092446..37096328hg38UCSC Ensembl
Innerchr8:36949964..36953846hg19UCSC Ensembl
Innerchr8:37069122..37073004hg18UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg383883
hg193883
hg183883
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2499612, nssv2499603, nssv2499608, nssv2499609, nssv2499606, nssv2499611, nssv2499607, nssv2499604, nssv2499605, nssv2499610
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)nsv971643
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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