A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214393



Internal ID20781433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:97867361..98081481hg38UCSC Ensembl
chr4:98788512..99002632hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38214121
hg19214121
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6379507
Supporting Variants
Samples
Known GenesSTPG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214393
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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