A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052579



Internal ID19141798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:43259815..43312501hg38UCSC Ensembl
Innerchr14:43729018..43781704hg19UCSC Ensembl
Innerchr14:42798768..42851454hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3852687
hg1952687
hg1852687
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3530223
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)nsv1052579
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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