A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18053113



Internal ID20620153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173278058..173278709hg38UCSC Ensembl
chr1:173247197..173247848hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38652
hg19652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6335210
Supporting Variants
Samples
Known GenesLOC100506023
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18053113
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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