A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5600770



Internal ID21549412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:32086493..32086930hg38UCSC Ensembl
chr14:32555699..32556136hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38438
hg19438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17083041
SamplesHG03065
Known GenesARHGAP5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5600770
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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