A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18064902



Internal ID20631942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:89009201..89013300hg38UCSC Ensembl
chr1:89474884..89478983hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332601
Supporting Variants
Samples
Known GenesGBP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18064902
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.10674


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