A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044278



Internal ID19133497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27834477..28195359hg38UCSC Ensembl
Innerchr14:28303683..28664565hg19UCSC Ensembl
Innerchr14:27373523..27734316hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38360883
hg19360883
hg18360794
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1860n100
Supporting Variantsnssv3528570
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)nsv1044278
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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