A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094966



Internal ID20662006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136866988..136868611hg38UCSC Ensembl
chr3:136585830..136587453hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg381624
hg191624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6370716
Supporting Variants
Samples
Known GenesNCK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094966
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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