A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486739



Internal ID21144292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27673216..27674155hg38UCSC Ensembl
chr13:28247353..28248292hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg38940
hg19940
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007513
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486739
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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