A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965726



Internal ID18600956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:53354228..53355029hg38UCSC Ensembl
Innerchr6:53219026..53219827hg19UCSC Ensembl
Innerchr6:53326985..53327786hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38802
hg19802
hg18802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2409365, nssv2409372, nssv2409370, nssv2409366, nssv2409369, nssv2409367, nssv2409373, nssv2409374, nssv2409371, nssv2409368
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)nsv965726
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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