A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490268



Internal ID21147821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:40215348..40371023hg38UCSC Ensembl
chr13:40789485..40945160hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38155676
hg19155676
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177533
Samples
Known GenesLINC00548, LINC00598
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490268
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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