A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18110263



Internal ID20677303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155774619..155778575hg38UCSC Ensembl
chr4:156695771..156699727hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg383957
hg193957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6390223
Supporting Variants
Samples
Known GenesGUCY1B3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18110263
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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