A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971692



Internal ID18606909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:106697022..106697522hg38UCSC Ensembl
Innerchr8:107709250..107709750hg19UCSC Ensembl
Innerchr8:107778426..107778926hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2515915, nssv2515917, nssv2515918, nssv2515914, nssv2515912, nssv2515913, nssv2515916, nssv2515911, nssv2515910, nssv2515909
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOXR1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv971692
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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