A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038014



Internal ID19127233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:25722339..25970188hg38UCSC Ensembl
Innerchr14:26191545..26439394hg19UCSC Ensembl
Innerchr14:25261385..25509234hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38247850
hg19247850
hg18247850
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3528532
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)nsv1038014
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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