A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203353



Internal ID20770393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59931701..59934700hg38UCSC Ensembl
chr20:58506756..58509755hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545827
Supporting Variants
Samples
Known GenesFAM217B, SYCP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203353
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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