A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045407



Internal ID19134626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27287258..27372740hg38UCSC Ensembl
Innerchr14:27756464..27841946hg19UCSC Ensembl
Innerchr14:26826304..26911786hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3885483
hg1985483
hg1885483
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1858n100
Supporting Variantsnssv3712270
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045407
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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