A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18110228



Internal ID20677268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:148505001..148507400hg38UCSC Ensembl
chr4:149426153..149428552hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6376680
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18110228
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00062


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