A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3746647



Internal ID19044928
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 StatusS
Merged Variantsnsv1025662
Supporting Variants
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)nssv3746647
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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