A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18115254



Internal ID20682294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:167732423..167923746hg38UCSC Ensembl
chr4:168653574..168844897hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38191324
hg19191324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6379751
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18115254
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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