A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487463



Internal ID21145016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109551901..109922600hg38UCSC Ensembl
chr13:110204248..110574947hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38370700
hg19370700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190937
Samples
Known GenesIRS2, LINC00676
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487463
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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