A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965698



Internal ID18254242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:27131919..27132537hg38UCSC Ensembl
Innerchr6:27099698..27100316hg19UCSC Ensembl
Innerchr6:27207677..27208295hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38619
hg19619
hg18619
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2399143, nssv2399137, nssv2399138, nssv2399142, nssv2399141, nssv2399139, nssv2399135, nssv2399134, nssv2399140, nssv2399136
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHIST1H2BJ
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965698
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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