A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974833



Internal ID18610042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:74325962..74373747hg38UCSC Ensembl
Innerchr16:74359860..74407645hg19UCSC Ensembl
Innerchr16:72917361..72965146hg18UCSC Ensembl
Cytoband16q22.3
Allele length
AssemblyAllele length
hg3847786
hg1947786
hg1847786
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2068383, nssv2068381, nssv2068386, nssv2068382, nssv2068379, nssv2068380, nssv2068384, nssv2068378, nssv2068387, nssv2068385
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC283922
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974833
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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