A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968870



Internal ID18604098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:5394865..5396925hg38UCSC Ensembl
Innerchr5:5394978..5397038hg19UCSC Ensembl
Innerchr5:5447978..5450038hg18UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg382061
hg192061
hg182061
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2345052, nssv2345050, nssv2345044, nssv2345046, nssv2345045, nssv2345047, nssv2345053, nssv2345049, nssv2345051, nssv2345048
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)nsv968870
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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