A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490051



Internal ID21147604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:75945652..76573909hg38UCSC Ensembl
chr13:76519788..77148044hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg38628258
hg19628257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18013087
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490051
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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