A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18043899



Internal ID20610939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76886356..76888256hg38UCSC Ensembl
chr18:74598312..74600212hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381901
hg191901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519044
Supporting Variants
Samples
Known GenesZNF236
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18043899
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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