A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18096314



Internal ID20663355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14939719..14946583hg38UCSC Ensembl
chr3:14981226..14988090hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg386865
hg196865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360069
Supporting Variants
Samples
Known GenesFGD5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18096314
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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