A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977673



Internal ID18612879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24904298..24910892hg38UCSC Ensembl
Innerchr15:25149445..25156039hg19UCSC Ensembl
Innerchr15:22700538..22707132hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg386595
hg196595
hg186595
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2008513, nssv2008514, nssv2008522, nssv2008521, nssv2008516, nssv2008520, nssv2008515, nssv2008517, nssv2008519, nssv2008518
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSNRPN
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977673
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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