A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968913



Internal ID18604141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:53199466..53213554hg38UCSC Ensembl
Innerchr5:52495296..52509384hg19UCSC Ensembl
Innerchr5:52531053..52545141hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3814089
hg1914089
hg1814089
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2355865, nssv2355863, nssv2355867, nssv2355871, nssv2355866, nssv2355870, nssv2355862, nssv2355868, nssv2355869, nssv2355864
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)nsv968913
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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