A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026175



Internal ID20593215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58530142..58535400hg38UCSC Ensembl
chr15:58822341..58827599hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg385259
hg195259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500416
Supporting Variants
Samples
Known GenesLIPC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026175
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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