A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516640



Internal ID20890001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13571104..13571873hg38UCSC Ensembl
chr18:13571103..13571872hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38770
hg19770
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039466
Samples
Known GenesLDLRAD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516640
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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