A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487406



Internal ID21144959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:33053023..33053478hg38UCSC Ensembl
chr13:33627160..33627615hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007743
Samples
Known GenesKL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487406
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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