A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490202



Internal ID21147755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34350626..34506807hg38UCSC Ensembl
chr13:34924763..35080944hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg38156182
hg19156182
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183596
Samples
Known GenesLINC00457
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490202
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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