A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18120593



Internal ID20687633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:97761547..98211971hg38UCSC Ensembl
chr4:98682698..99133122hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38450425
hg19450425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6387914
Supporting Variants
Samples
Known GenesSTPG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18120593
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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