A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065523



Internal ID20632563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86407647..86409956hg38UCSC Ensembl
chr1:86873330..86875639hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg382310
hg192310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6329752
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065523
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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