A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476566



Internal ID21134119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87787766..87821561hg38UCSC Ensembl
chr13:88440021..88473816hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3833796
hg1933796
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196438
Samples
Known GenesLINC00397
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476566
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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