A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18017810



Internal ID20584850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:32154701..32158300hg38UCSC Ensembl
chr14:32623907..32627506hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6480879
Supporting Variants
Samples
Known GenesARHGAP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18017810
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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