A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037689



Internal ID18780220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:100024646..100753868hg38UCSC Ensembl
Innerchr11:99895378..100624599hg19UCSC Ensembl
Innerchr11:99400588..100129809hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38729223
hg19729222
hg18729222
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1265n100
Supporting Variantsnssv3505255
Samples
Known GenesARHGAP42, CNTN5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037689
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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