A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037958



Internal ID18780489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:24517702..24612159hg38UCSC Ensembl
Innerchr10:24806631..24901088hg19UCSC Ensembl
Innerchr10:24846637..24941094hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3894458
hg1994458
hg1894458
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3504458
Samples
Known GenesARHGAP21, KIAA1217
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037958
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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