A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965699



Internal ID18600929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:27863826..27865796hg38UCSC Ensembl
Innerchr6:27831604..27833574hg19UCSC Ensembl
Innerchr6:27939583..27941553hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg381971
hg191971
hg181971
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2400060, nssv2400058, nssv2400052, nssv2400057, nssv2400053, nssv2400061, nssv2400059, nssv2400055, nssv2400056, nssv2400054
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHIST1H2AL
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965699
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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