A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18020531



Internal ID20587571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:67971144..67983418hg38UCSC Ensembl
chr14:68437861..68450135hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg3812275
hg1912275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6483676
Supporting Variants
Samples
Known GenesRAD51B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18020531
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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