A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18109497



Internal ID20676537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:14632359..14632774hg38UCSC Ensembl
chr4:14633983..14634398hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38416
hg19416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6373016
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18109497
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00078


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