A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2017883



Internal ID17767687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:37489207..37491094hg38UCSC Ensembl
Innerchr15:37781408..37783295hg19UCSC Ensembl
Innerchr15:35568700..35570587hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg381888
hg191888
hg181888
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv977701
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)nssv2017883
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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