A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494455



Internal ID21152008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90820729..90821281hg38UCSC Ensembl
chr13:91472983..91473535hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38553
hg19553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18014481
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494455
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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