A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18092426



Internal ID20659467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101841479..101844858hg38UCSC Ensembl
chr3:101560323..101563702hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg383380
hg193380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367442
Supporting Variants
Samples
Known GenesNFKBIZ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18092426
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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