A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968966



Internal ID18604194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:98409942..98416110hg38UCSC Ensembl
Innerchr5:97745646..97751814hg19UCSC Ensembl
Innerchr5:97773546..97779714hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg386169
hg196169
hg186169
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2370616, nssv2370618, nssv2370623, nssv2370625, nssv2370617, nssv2370621, nssv2370622, nssv2370620, nssv2370624, nssv2370619
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)nsv968966
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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