A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493961



Internal ID21151514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:84482549..84491045hg38UCSC Ensembl
chr13:85056684..85065180hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg388497
hg198497
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18014934
Samples
Known GenesLINC00333
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493961
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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