A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18105040



Internal ID20672080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99512243..99524462hg38UCSC Ensembl
chr3:99231087..99243306hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3812220
hg1912220
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357081
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18105040
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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