A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3505255



Internal ID18456850
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 StatusS
Merged Variantsnsv1037689
Supporting Variants
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)nssv3505255
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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