A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3505367



Internal ID18803648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:120359534..120414894hg38UCSC Ensembl
Innerchr11:120230243..120285603hg19UCSC Ensembl
Innerchr11:119735453..119790813hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3855361
hg1955361
hg1855361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036694
Supporting Variants
Samples
Known GenesARHGEF12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3505367
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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