A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710705



Internal ID19008986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:91442361..91485832hg38UCSC Ensembl
Innerchr11:91175527..91218998hg19UCSC Ensembl
Innerchr11:90815175..90858646hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3843472
hg1943472
hg1843472
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046616
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3710705
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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