A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18117175



Internal ID20684215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4689434..4695528hg38UCSC Ensembl
chr4:4691161..4697255hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg386095
hg196095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372905
Supporting Variants
Samples
Known GenesSTX18-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18117175
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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