A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068885



Internal ID20635925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:39219625..39220543hg38UCSC Ensembl
chr20:37848268..37849186hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38919
hg19919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526543
Supporting Variants
Samples
Known GenesLOC339568
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068885
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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