A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195459



Internal ID20762499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101182872..101351952hg38UCSC Ensembl
chr15:101723077..101892157hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38169081
hg19169081
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504047
Supporting Variants
Samples
Known GenesCHSY1, LOC100507472, PCSK6, SNRPA1, VIMP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195459
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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