A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5942787



Internal ID22718230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93948637..93948732hg38UCSC Ensembl
chr14:94414983..94415078hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372325
Samples
Known GenesASB2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5942787
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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