A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484971



Internal ID21142524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109545910..109546285hg38UCSC Ensembl
chr13:110198257..110198632hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007956
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484971
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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