A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203305



Internal ID20770345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34474201..34476900hg38UCSC Ensembl
chr20:33062006..33064705hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527052
Supporting Variants
Samples
Known GenesITCH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203305
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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