A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046588



Internal ID18789119
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 StatusM
Merged Variants
Supporting Variantsnssv3509025
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)nsv1046588
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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