A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2025150



Internal ID17883658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57555984..57556681hg38UCSC Ensembl
Innerchr15:57848182..57848879hg19UCSC Ensembl
Innerchr15:55635474..55636171hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38698
hg19698
hg18698
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv984075
Supporting Variants
SamplesHGDP01307
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)nssv2025150
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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