A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17455969



Internal ID22513846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35690752..35692097hg38UCSC Ensembl
chr14:36159958..36161303hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg381346
hg191346
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866290
Supporting Variants
Samples
Known GenesRALGAPA1, RALGAPA1P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17455969
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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