A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970092



Internal ID18605316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:27209971..27213955hg38UCSC Ensembl
Innerchr6:27177750..27181734hg19UCSC Ensembl
Innerchr6:27285729..27289713hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg383985
hg193985
hg183985
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2400218, nssv2400220, nssv2400225, nssv2400224, nssv2400217, nssv2400222, nssv2400226, nssv2400219, nssv2400223, nssv2400221
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)nsv970092
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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