A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490795



Internal ID21148348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113751913..113752233hg38UCSC Ensembl
chr13:114454886..114455206hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007782
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490795
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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