A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18097847



Internal ID20664887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182216446..182220909hg38UCSC Ensembl
chr3:181934234..181938697hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg384464
hg194464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6370782
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18097847
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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