A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204287



Internal ID20771327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:64775971..64788461hg38UCSC Ensembl
chr1:65241654..65254144hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3812491
hg1912491
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6333652
Supporting Variants
Samples
Known GenesRAVER2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204287
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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