A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3521950



Internal ID18820231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107353032..107368390hg38UCSC Ensembl
Innerchr11:107223758..107239116hg19UCSC Ensembl
Innerchr11:106728968..106744326hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3815359
hg1915359
hg1815359
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035610
Supporting Variants
Samples
Known GenesCWF19L2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3521950
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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