A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488260



Internal ID21145813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95083876..95307720hg38UCSC Ensembl
chr13:95736130..95959974hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38223845
hg19223845
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193032
Samples
Known GenesABCC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488260
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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