A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482497



Internal ID21140050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:40472848..40476631hg38UCSC Ensembl
chr13:41046985..41050768hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg383784
hg193784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18008901
Samples
Known GenesLINC00598
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482497
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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