A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065182



Internal ID20632222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:92398281..92398887hg38UCSC Ensembl
chr1:92863838..92864444hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38607
hg19607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6325940
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065182
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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