A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974753



Internal ID18263276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:5236416..5296073hg38UCSC Ensembl
Innerchr16:5286417..5346074hg19UCSC Ensembl
Innerchr16:5226418..5286075hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3859658
hg1959658
hg1859658
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2041454, nssv2041456, nssv2041457, nssv2041453, nssv2041451, nssv2041449, nssv2041458, nssv2041455, nssv2041452, nssv2041450
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)nsv974753
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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