A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980273



Internal ID18615473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:169770180..169770924hg38UCSC Ensembl
Innerchr4:170691331..170692075hg19UCSC Ensembl
Innerchr4:170927906..170928650hg18UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38745
hg19745
hg18745
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2341536, nssv2341533, nssv2341530, nssv2341538, nssv2341534, nssv2341537, nssv2341535, nssv2341529, nssv2341531, nssv2341532
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)nsv980273
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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