A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970074



Internal ID18605298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:5803927..5811188hg38UCSC Ensembl
Innerchr6:5804160..5811421hg19UCSC Ensembl
Innerchr6:5749159..5756420hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg387262
hg197262
hg187262
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2393188, nssv2393189, nssv2393194, nssv2393190, nssv2393197, nssv2393192, nssv2393191, nssv2393196, nssv2393193, nssv2393195
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)nsv970074
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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