A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981199



Internal ID18616398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:156658987..156678223hg38UCSC Ensembl
Innerchr6:156980121..156999357hg19UCSC Ensembl
Innerchr6:157021813..157041049hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3819237
hg1919237
hg1819237
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2426864, nssv2426859, nssv2426858, nssv2426861, nssv2426860, nssv2426865, nssv2426866, nssv2426863, nssv2426857, nssv2426862
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)nsv981199
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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