A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489361



Internal ID21146914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:80440801..80443400hg38UCSC Ensembl
chr13:81014936..81017535hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18013555
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489361
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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