A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969419



Internal ID18604646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:73372554..73377049hg38UCSC Ensembl
Innerchr6:74082277..74086772hg19UCSC Ensembl
Innerchr6:74138998..74143493hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg384496
hg194496
hg184496
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2413418, nssv2413421, nssv2413425, nssv2413417, nssv2413416, nssv2413420, nssv2413424, nssv2413423, nssv2413419, nssv2413422
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)nsv969419
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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