A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3512662



Internal ID18810943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3397110..3590539hg38UCSC Ensembl
Innerchr11:3418340..3611769hg19UCSC Ensembl
Innerchr11:3374916..3568345hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38193430
hg19193430
hg18193430
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042884
Supporting Variants
Samples
Known GenesLOC650368
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3512662
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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