A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067183



Internal ID20634223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25663068..25680038hg38UCSC Ensembl
chr20:25643704..25660674hg19UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3816971
hg1916971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524633
Supporting Variants
Samples
Known GenesZNF337
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067183
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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