A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042666



Internal ID19131885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:39773696..39824296hg38UCSC Ensembl
Innerchr14:40242900..40293500hg19UCSC Ensembl
Innerchr14:39312651..39363251hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3850601
hg1950601
hg1850601
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1875n100
Supporting Variantsnssv3530131
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)nsv1042666
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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