A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18104266



Internal ID20671306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97987601..98023300hg38UCSC Ensembl
chr3:97706445..97742144hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3835700
hg1935700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6370496
Supporting Variants
Samples
Known GenesGABRR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18104266
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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