A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495564



Internal ID21153117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75538079..75539753hg38UCSC Ensembl
chr14:76004422..76006096hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381675
hg191675
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182312
Samples
Known GenesBATF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495564
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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