A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18122406



Internal ID20689446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:88716448..88719199hg38UCSC Ensembl
chr4:89637599..89640350hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg382752
hg192752
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6375965
Supporting Variants
Samples
Known GenesFAM13A-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18122406
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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