A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18105045



Internal ID20672085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9955682..9960394hg38UCSC Ensembl
chr3:9997366..10002078hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg384713
hg194713
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6364217
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18105045
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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