A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18066099



Internal ID20633139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9518927..9522325hg38UCSC Ensembl
chr1:9578986..9582384hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg383399
hg193399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6329397
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18066099
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00177


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