A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182034



Internal ID20749074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101452720..101638270hg38UCSC Ensembl
chr13:102105071..102290620hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38185551
hg19185550
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6491389
Supporting Variants
Samples
Known GenesITGBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182034
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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