A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968184



Internal ID18603412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:65414543..65420817hg38UCSC Ensembl
Innerchr5:64710370..64716644hg19UCSC Ensembl
Innerchr5:64746126..64752400hg18UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg386275
hg196275
hg186275
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2359185, nssv2359181, nssv2359182, nssv2359180, nssv2359179, nssv2359186, nssv2359183, nssv2359184, nssv2359188, nssv2359187
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesADAMTS6
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968184
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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