A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039738



Internal ID20606778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36027941..36028303hg38UCSC Ensembl
chr18:33607904..33608266hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38363
hg19363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530078
Supporting Variants
Samples
Known GenesRPRD1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039738
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00097


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