A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065506



Internal ID20632546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86304524..86317092hg38UCSC Ensembl
chr1:86770207..86782775hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3812569
hg1912569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6327487
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065506
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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