A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044189



Internal ID20611229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76431440..76434772hg38UCSC Ensembl
chr18:74143396..74146728hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg383333
hg193333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530934
Supporting Variants
Samples
Known GenesZNF516
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044189
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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