A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2018802



Internal ID17832117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:35121193..35124561hg38UCSC Ensembl
Innerchr15:35413394..35416762hg19UCSC Ensembl
Innerchr15:33200686..33204054hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg383369
hg193369
hg183369
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv976920
Supporting Variants
SamplesHGDP00998
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)nssv2018802
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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