A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533434



Internal ID20906795
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 StatusM
Merged Variants
Supporting Variantsnssv18039955
Samples
Known GenesRNF125
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533434
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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