A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3473940



Internal ID19065733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15189803..15224029hg38UCSC Ensembl
Innerchr1:15516299..15550525hg19UCSC Ensembl
Innerchr1:15388886..15423112hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3834227
hg1934227
hg1834227
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005708
Supporting Variants
Samples
Known GenesTMEM51
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3473940
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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