A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494189



Internal ID21151742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:65997457..65998252hg38UCSC Ensembl
chr13:66571589..66572384hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg38796
hg19796
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18011568
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494189
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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