A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18056582



Internal ID20623622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:200024560..200025537hg38UCSC Ensembl
chr1:199993688..199994665hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38978
hg19978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331321
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18056582
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


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