A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3505784



Internal ID18457379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1883459..1939958hg38UCSC Ensembl
Innerchr11:1904689..1961188hg19UCSC Ensembl
Innerchr11:1861265..1917764hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3856500
hg1956500
hg1856500
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039289
Supporting Variants
Samples
Known GenesLSP1, TNNT3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3505784
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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