A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068003



Internal ID20635043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35569912..35571232hg38UCSC Ensembl
chr20:34157842..34159162hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg381321
hg191321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522312
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068003
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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