A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18058550



Internal ID20625590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:229650479..229836606hg38UCSC Ensembl
chr1:229786226..229972353hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg38186128
hg19186128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6324510
Supporting Variants
Samples
Known GenesURB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18058550
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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