A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487645



Internal ID21145198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34836201..34843900hg38UCSC Ensembl
chr14:35305407..35313106hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg387700
hg197700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18017448
Samples
Known GenesBAZ1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487645
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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