A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980768



Internal ID18269282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:178040633..178043443hg38UCSC Ensembl
Innerchr5:177467634..177470444hg19UCSC Ensembl
Innerchr5:177400240..177403050hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg382811
hg192811
hg182811
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2705402, nssv2705407, nssv2705409, nssv2705404, nssv2705403, nssv2705408, nssv2705405, nssv2705406, nssv2705410, nssv2705401
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFAM153C
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv980768
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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