A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044011



Internal ID20611051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:75208504..75208758hg38UCSC Ensembl
chr18:72920459..72920713hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38255
hg19255
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524673
Supporting Variants
Samples
Known GenesZADH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044011
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00694


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