A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18105538



Internal ID20672578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97770085..97901781hg38UCSC Ensembl
chr3:97488929..97620625hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38131697
hg19131697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6370580
Supporting Variants
Samples
Known GenesARL6, CRYBG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18105538
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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