A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18059675



Internal ID20626715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244812566..244813939hg38UCSC Ensembl
chr1:244975868..244977241hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg381374
hg191374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331099
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18059675
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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