A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039448



Internal ID20606488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13248481..13344059hg38UCSC Ensembl
chr18:13248480..13344058hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3895579
hg1995579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522780
Supporting Variants
Samples
Known GenesLDLRAD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039448
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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