A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18115539



Internal ID20682579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28904498..28904967hg38UCSC Ensembl
chr4:28906120..28906589hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6363020
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18115539
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00069


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