A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977898



Internal ID18613103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:2657895..2671502hg38UCSC Ensembl
Innerchr16:2707896..2721503hg19UCSC Ensembl
Innerchr16:2647897..2661504hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3813608
hg1913608
hg1813608
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2042568, nssv2042563, nssv2042570, nssv2042569, nssv2042571, nssv2042564, nssv2042566, nssv2042567, nssv2042572, nssv2042565
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesERVK13-1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977898
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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