A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18110605



Internal ID20677645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:127017462..127018052hg38UCSC Ensembl
chr4:127938617..127939207hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6375957
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18110605
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00061


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