A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046643



Internal ID18789174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22386647..22560975hg38UCSC Ensembl
Innerchr14:22855050..23029875hg19UCSC Ensembl
Innerchr14:21924890..22099715hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38174329
hg19174826
hg18174826
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3532323
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)nsv1046643
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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