A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18117346



Internal ID20684386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52302301..52304200hg38UCSC Ensembl
chr4:53168467..53170366hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6376433
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18117346
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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