A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18058721



Internal ID20625761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23201719..23207677hg38UCSC Ensembl
chr1:23528212..23534170hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg385959
hg195959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317216
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18058721
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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