A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067571



Internal ID20634611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40372801..40373600hg38UCSC Ensembl
chr20:39001441..39002240hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551661
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067571
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0004


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