A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516812



Internal ID20890173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13313794..13317167hg38UCSC Ensembl
chr18:13313793..13317166hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg383374
hg193374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039450
Samples
Known GenesLDLRAD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516812
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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