A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18057224



Internal ID20624264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:209001213..209004282hg38UCSC Ensembl
chr1:209174558..209177627hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg383070
hg193070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6325473
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18057224
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00038


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