A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485917



Internal ID21143470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95238075..95295847hg38UCSC Ensembl
chr13:95890329..95948101hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3857773
hg1957773
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182387
Samples
Known GenesABCC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485917
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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