A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18058076



Internal ID20625116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:218906459..218907206hg38UCSC Ensembl
chr1:219079801..219080548hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38748
hg19748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6319411
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18058076
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00071


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