A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005257



Internal ID18747788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:85978443..86004316hg38UCSC Ensembl
Innerchr4:86899596..86925469hg19UCSC Ensembl
Innerchr4:87118620..87144493hg18UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg3825874
hg1925874
hg1825874
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3633904
Samples
Known GenesARHGAP24
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005257
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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