A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531678



Internal ID18829959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:47358234..47410004hg38UCSC Ensembl
Innerchr14:47827437..47879207hg19UCSC Ensembl
Innerchr14:46897187..46948957hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3851771
hg1951771
hg1851771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037655
Supporting Variants
Samples
Known GenesMDGA2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3531678
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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