A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045746



Internal ID19134965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:40290622..40383342hg38UCSC Ensembl
Innerchr14:40759826..40852546hg19UCSC Ensembl
Innerchr14:39829576..39922296hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3892721
hg1992721
hg1892721
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3530144, nssv3530145
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)nsv1045746
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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