A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202005



Internal ID20769046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:195638885..195756947hg38UCSC Ensembl
chr1:195608015..195726077hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg38118063
hg19118063
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6316040
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202005
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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