A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18108325



Internal ID20675366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:118322501..118324400hg38UCSC Ensembl
chr4:119243656..119245555hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6392353
Supporting Variants
Samples
Known GenesPRSS12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18108325
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00301


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