A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523462



Internal ID20896823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:71763262..71763957hg38UCSC Ensembl
chr18:69430498..69431193hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38696
hg19696
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18043760
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523462
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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