A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522780



Internal ID20896141
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 StatusM
Merged Variants
Supporting Variantsnssv18039448
Samples
Known GenesLDLRAD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522780
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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