A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978420



Internal ID18266939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:38854047..38861611hg38UCSC Ensembl
Innerchr17:37010300..37017864hg19UCSC Ensembl
Innerchr17:34263826..34271390hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg387565
hg197565
hg187565
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2093520, nssv2093513, nssv2093518, nssv2093519, nssv2093512, nssv2093515, nssv2093517, nssv2093516, nssv2093514, nssv2093521
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)nsv978420
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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