A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564469



Internal ID16351878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:40840951..41077979hg38UCSC Ensembl
Innerchr14:41310156..41547184hg19UCSC Ensembl
Innerchr14:40379906..40616934hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38237029
hg19237029
hg18237029
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv826665
Samples
Known GenesLOC644919
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564469
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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