A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564454



Internal ID16351863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:40148961..40232475hg38UCSC Ensembl
Innerchr14:40618165..40701679hg19UCSC Ensembl
Innerchr14:39687916..39771429hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3883515
hg1983515
hg1883514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv826656
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564454
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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