A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040487



Internal ID19129706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:36301607..36336415hg38UCSC Ensembl
Innerchr14:36770813..36805621hg19UCSC Ensembl
Innerchr14:35840564..35875372hg18UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg3834809
hg1934809
hg1834809
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3528621
Samples
Known GenesMBIP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040487
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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