A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481802



Internal ID21139355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35572544..35573076hg38UCSC Ensembl
chr14:36041750..36042282hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18017295
Samples
Known GenesRALGAPA1, RALGAPA1P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481802
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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