A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18057094



Internal ID20624134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206488080..206489386hg38UCSC Ensembl
chr1:206661417..206662719hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg381307
hg191303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6325191
Supporting Variants
Samples
Known GenesIKBKE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18057094
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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