A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533462



Internal ID20906823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:75260125..75265997hg38UCSC Ensembl
chr18:72972080..72977952hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg385873
hg195873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044017
Samples
Known GenesTSHZ1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533462
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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