A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18053511



Internal ID20620551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159347295..159354947hg38UCSC Ensembl
chr1:159317085..159324737hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg387653
hg197653
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6330065
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18053511
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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