A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18040402



Internal ID20607442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24285002..24291319hg38UCSC Ensembl
chr18:21864966..21871283hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg386318
hg196318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524032
Supporting Variants
Samples
Known GenesOSBPL1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18040402
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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