A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052296



Internal ID19141515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:43348906..43772103hg38UCSC Ensembl
Innerchr14:43818109..44241306hg19UCSC Ensembl
Innerchr14:42887859..43311056hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38423198
hg19423198
hg18423198
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1890n100
Supporting Variantsnssv3530229
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)nsv1052296
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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