A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525294



Internal ID15452587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35609510..35655129hg38UCSC Ensembl
Innerchr14:36078716..36124335hg19UCSC Ensembl
Innerchr14:35148467..35194086hg18UCSC Ensembl
Innerchr14:35148467..35194086hg17UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3845620
hg1945620
hg1845620
hg1745620
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701400
Samples
Known GenesRALGAPA1, RALGAPA1P
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525294
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer