A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203315



Internal ID20770355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35442749..35443715hg38UCSC Ensembl
chr20:34030557..34031523hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38967
hg19967
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531397
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203315
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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