A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18096995



Internal ID20664035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16372809..16374261hg38UCSC Ensembl
chr3:16414316..16415768hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg381453
hg191453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6363602
Supporting Variants
Samples
Known GenesRFTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18096995
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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