A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2008515



Internal ID17803667
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 StatusS
Merged Variantsnsv977673
Supporting Variants
SamplesHGDP00778
Known GenesSNRPN
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2008515
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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