A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18097673



Internal ID20664713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185281477..185283780hg38UCSC Ensembl
chr3:184999265..185001568hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg382304
hg192304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6358021
Supporting Variants
Samples
Known GenesMAP3K13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18097673
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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