A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2018708



Internal ID17769623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:35081340..35085179hg38UCSC Ensembl
Innerchr15:35373541..35377380hg19UCSC Ensembl
Innerchr15:33160833..33164672hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg383840
hg193840
hg183840
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv977700
Supporting Variants
SamplesHGDP00542
Known Genes
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)nssv2018708
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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