A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984354



Internal ID18619541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:74552260..74552760hg38UCSC Ensembl
Innerchr16:74586158..74586658hg19UCSC Ensembl
Innerchr16:73143659..73144159hg18UCSC Ensembl
Cytoband16q22.3
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2066870, nssv2066871, nssv2066868, nssv2066866, nssv2066867, nssv2066874, nssv2066873, nssv2066869, nssv2066872, nssv2066875
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesGLG1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv984354
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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