A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3509025



Internal ID18460620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:48582209..48598124hg38UCSC Ensembl
Innerchr10:49790254..49806169hg19UCSC Ensembl
Innerchr10:49460260..49476175hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3815916
hg1915916
hg1815916
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046588
Supporting Variants
Samples
Known GenesARHGAP22
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3509025
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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