A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3503152



Internal ID18801433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107150265..107327455hg38UCSC Ensembl
Innerchr11:107020991..107198181hg19UCSC Ensembl
Innerchr11:106526201..106703391hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38177191
hg19177191
hg18177191
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035911
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)nssv3503152
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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