A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980207



Internal ID18615407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:62510742..62511839hg38UCSC Ensembl
Innerchr4:63376460..63377557hg19UCSC Ensembl
Innerchr4:63059055..63060152hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg381098
hg191098
hg181098
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2319594, nssv2319588, nssv2319595, nssv2319591, nssv2319590, nssv2319592, nssv2319587, nssv2319596, nssv2319589, nssv2319593
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)nsv980207
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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