A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18114486



Internal ID20681526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16439656..16440123hg38UCSC Ensembl
chr4:16441279..16441746hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38468
hg19468
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371225
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18114486
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00042


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