A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3520608



Internal ID18818889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:120368253..120443469hg38UCSC Ensembl
Innerchr11:120238962..120314178hg19UCSC Ensembl
Innerchr11:119744172..119819388hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3875217
hg1975217
hg1875217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051672
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)nssv3520608
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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