A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490887



Internal ID21148440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:78422701..78424800hg38UCSC Ensembl
chr13:78996836..78998935hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18013034
Samples
Known GenesRNF219-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490887
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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