A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980699



Internal ID18269213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:95814091..95815194hg38UCSC Ensembl
Innerchr5:95149795..95150898hg19UCSC Ensembl
Innerchr5:95175551..95176654hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg381104
hg191104
hg181104
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2369929, nssv2369931, nssv2369930, nssv2369927, nssv2369935, nssv2369936, nssv2369933, nssv2369932, nssv2369934, nssv2369928
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesGLRX
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv980699
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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