A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039955



Internal ID20606995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:32057732..32061042hg38UCSC Ensembl
chr18:29637695..29641005hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg383311
hg193311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533434
Supporting Variants
Samples
Known GenesRNF125
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039955
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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