A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3706395



Internal ID19004676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3400993..3600393hg38UCSC Ensembl
Innerchr11:3422223..3621623hg19UCSC Ensembl
Innerchr11:3378799..3578199hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38199401
hg19199401
hg18199401
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048151
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)nssv3706395
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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