A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18117341



Internal ID20684381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52233601..52316900hg38UCSC Ensembl
chr4:53099767..53183066hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3883300
hg1983300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6377169
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18117341
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00092


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