A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099358



Internal ID20666398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31905368..32199484hg38UCSC Ensembl
chr3:31946860..32240976hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38294117
hg19294117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368302
Supporting Variants
Samples
Known GenesGPD1L, OSBPL10, ZNF860
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099358
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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