A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035573



Internal ID19124792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105563288..105733027hg38UCSC Ensembl
Innerchr14:106029625..106199364hg19UCSC Ensembl
Innerchr14:105100670..105270409hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38169740
hg19169740
hg18169740
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1983n100
Supporting Variantsnssv3529826, nssv3529825
Samples
Known GenesELK2AP, MIR8071-1, MIR8071-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035573
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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