A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490090



Internal ID21147643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79405601..79406100hg38UCSC Ensembl
chr13:79979736..79980235hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18012854
Samples
Known GenesRBM26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490090
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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