A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044217



Internal ID20611257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76596151..76596612hg38UCSC Ensembl
chr18:74308108..74308569hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38462
hg19462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6520626
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044217
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00042


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