A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18042075



Internal ID20609115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:42392478..42392952hg38UCSC Ensembl
chr18:39972443..39972917hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38475
hg19475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530689
Supporting Variants
Samples
Known GenesLINC00907
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18042075
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00081


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