A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18104376



Internal ID20671416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:69212344..69222727hg38UCSC Ensembl
chr3:69261495..69271878hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3810384
hg1910384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6373896
Supporting Variants
Samples
Known GenesFRMD4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18104376
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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