A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2019364



Internal ID17865266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:40760551..40761148hg38UCSC Ensembl
Innerchr15:41052749..41053346hg19UCSC Ensembl
Innerchr15:38840041..38840638hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38598
hg19598
hg18598
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv977702
Supporting Variants
SamplesHGDP01284
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)nssv2019364
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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