A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974599



Internal ID18609810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:75740727..75808801hg38UCSC Ensembl
Innerchr15:76033068..76101142hg19UCSC Ensembl
Innerchr15:73820123..73888197hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3868075
hg1968075
hg1868075
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2032118, nssv2032117, nssv2032114, nssv2032122, nssv2032116, nssv2032113, nssv2032120, nssv2032121, nssv2032115, nssv2032119
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMIR4313
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974599
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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