A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978177



Internal ID18266696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88165314..88194603hg38UCSC Ensembl
Innerchr16:88198920..88228209hg19UCSC Ensembl
Innerchr16:86756421..86785710hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3829290
hg1929290
hg1829290
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2070112, nssv2070114, nssv2070111, nssv2070115, nssv2070113, nssv2070110, nssv2070109, nssv2070107, nssv2070116, nssv2070108
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)nsv978177
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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