A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928539



Internal ID22703780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92929294..92929373hg38UCSC Ensembl
chr14:93395639..93395718hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376901
Samples
Known GenesCHGA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928539
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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