A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978156



Internal ID18613361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:57601369..57606503hg38UCSC Ensembl
Innerchr16:57635281..57640415hg19UCSC Ensembl
Innerchr16:56192782..56197916hg18UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg385135
hg195135
hg185135
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2063498, nssv2063506, nssv2063505, nssv2063499, nssv2063500, nssv2063507, nssv2063504, nssv2063501, nssv2063503, nssv2063502
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)nsv978156
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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