A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026099



Internal ID20593139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:61524334..61525903hg38UCSC Ensembl
chr15:61816533..61818102hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381570
hg191570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502828
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026099
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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