A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564464



Internal ID16351873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:40488338..41402672hg38UCSC Ensembl
Innerchr14:40957542..41871875hg19UCSC Ensembl
Innerchr14:40027292..40941625hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38914335
hg19914334
hg18914334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv826663
Samples
Known GenesLOC644919
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564464
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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