A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18110262



Internal ID20677302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155767437..155768163hg38UCSC Ensembl
chr4:156688589..156689315hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38727
hg19727
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6376056
Supporting Variants
Samples
Known GenesGUCY1B3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18110262
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00045


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