A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3506692



Internal ID18458287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:14668177..14714291hg38UCSC Ensembl
Innerchr11:14689723..14735837hg19UCSC Ensembl
Innerchr11:14646299..14692413hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3846115
hg1946115
hg1846115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042405
Supporting Variants
Samples
Known GenesPDE3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3506692
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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