A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968964



Internal ID18604192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:98339445..98340339hg38UCSC Ensembl
Innerchr5:97675149..97676043hg19UCSC Ensembl
Innerchr5:97703053..97703947hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38895
hg19895
hg18895
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2370429, nssv2370424, nssv2370426, nssv2370431, nssv2370422, nssv2370427, nssv2370425, nssv2370428, nssv2370423, nssv2370430
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)nsv968964
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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