A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039457



Internal ID20606497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13451418..13459657hg38UCSC Ensembl
chr18:13451417..13459656hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg388240
hg198240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531254
Supporting Variants
Samples
Known GenesLDLRAD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039457
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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