A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3514501



Internal ID18812782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:120368253..120405664hg38UCSC Ensembl
Innerchr11:120238962..120276373hg19UCSC Ensembl
Innerchr11:119744172..119781583hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3837412
hg1937412
hg1837412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047982
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)nssv3514501
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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