A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483613



Internal ID21141166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95271837..95500763hg38UCSC Ensembl
chr13:95924091..96153017hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38228927
hg19228927
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190060
Samples
Known GenesABCC4, CLDN10, CLDN10-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483613
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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