A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18105540



Internal ID20672580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97787436..97787960hg38UCSC Ensembl
chr3:97506280..97506804hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38525
hg19525
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6365907
Supporting Variants
Samples
Known GenesARL6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18105540
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00032


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