A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2022810



Internal ID17786840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:47043925..47104263hg38UCSC Ensembl
Innerchr15:47336123..47396461hg19UCSC Ensembl
Innerchr15:45123415..45183753hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3860339
hg1960339
hg1860339
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv977714
Supporting Variants
SamplesHGDP00665
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)nssv2022810
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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