A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025662



Internal ID19114880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:142965889..143118671hg38UCSC Ensembl
Innerchr5:142345454..142498236hg19UCSC Ensembl
Innerchr5:142325638..142478429hg18UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38152783
hg19152783
hg18152792
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3746647
Samples
Known GenesARHGAP26
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025662
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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