A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978010



Internal ID18266529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88009231..88046385hg38UCSC Ensembl
Innerchr16:88042837..88079991hg19UCSC Ensembl
Innerchr16:86600338..86637492hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3837155
hg1937155
hg1837155
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2069986, nssv2069982, nssv2069987, nssv2069980, nssv2069984, nssv2069983, nssv2069978, nssv2069985, nssv2069981, nssv2069979
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesBANP
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv978010
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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