A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977959



Internal ID18613164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:31936022..31951007hg38UCSC Ensembl
Innerchr16:31947343..31962328hg19UCSC Ensembl
Innerchr16:31854844..31869829hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3814986
hg1914986
hg1814986
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2055559, nssv2055563, nssv2055561, nssv2055566, nssv2055560, nssv2055557, nssv2055564, nssv2055558, nssv2055565, nssv2055562
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)nsv977959
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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