A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18042071



Internal ID20609111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:42365645..42366376hg38UCSC Ensembl
chr18:39945610..39946341hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38732
hg19732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533076
Supporting Variants
Samples
Known GenesLINC00907
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18042071
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00034


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