A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18120184



Internal ID20687224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:72402995..72403400hg38UCSC Ensembl
chr4:73268712..73269117hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6383425
Supporting Variants
Samples
Known GenesADAMTS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18120184
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00123


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