A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067553



Internal ID20634593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40134437..40138415hg38UCSC Ensembl
chr20:38763078..38767056hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg383979
hg193979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543817
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067553
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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