A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18121674



Internal ID20688714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:85871029..85871633hg38UCSC Ensembl
chr4:86792182..86792786hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38605
hg19605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6378664
Supporting Variants
Samples
Known GenesARHGAP24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18121674
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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