A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183984



Internal ID20751024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85303001..85407200hg38UCSC Ensembl
chr13:85877136..85981335hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38104200
hg19104200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6488816
Supporting Variants
Samples
Known GenesLINC00351
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183984
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0002


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