A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965051



Internal ID18600286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:181467855..181478259hg38UCSC Ensembl
Innerchr5:180894856..180905260hg19UCSC Ensembl
Innerchr5:180827462..180837969hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3810405
hg1910405
hg1810508
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv69n82
Supporting Variantsnssv2703935, nssv2703941, nssv2703937, nssv2703942, nssv2703938, nssv2703940, nssv2703943, nssv2703939, nssv2703936, nssv2703934
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965051
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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