A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052683



Internal ID20619723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:164254096..164261397hg38UCSC Ensembl
chr1:164223333..164230634hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg387302
hg197302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6316180
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052683
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0002


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