A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039528



Internal ID20606568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:25208638..25210743hg38UCSC Ensembl
chr18:22788602..22790707hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg382106
hg192106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6517184
Supporting Variants
Samples
Known GenesZNF521
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039528
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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