A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202234



Internal ID20769274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38087393..38229833hg38UCSC Ensembl
chr20:36715795..36858235hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38142441
hg19142441
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524545
Supporting Variants
Samples
Known GenesKIAA1755, RPRD1B, TGM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202234
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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