A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026173



Internal ID20593213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58457249..58461496hg38UCSC Ensembl
chr15:58749448..58753695hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg384248
hg194248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513023
Supporting Variants
Samples
Known GenesLIPC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026173
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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