A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964908



Internal ID18253458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:95499022..95501060hg38UCSC Ensembl
Innerchr5:94834726..94836764hg19UCSC Ensembl
Innerchr5:94860482..94862520hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg382039
hg192039
hg182039
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2368946, nssv2368941, nssv2368943, nssv2368947, nssv2368944, nssv2368949, nssv2368945, nssv2368950, nssv2368948, nssv2368942
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesTTC37
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964908
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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