A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564888



Internal ID16352297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:62238616..62276894hg38UCSC Ensembl
Innerchr14:62705334..62743612hg19UCSC Ensembl
Innerchr14:61775087..61813365hg18UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3838279
hg1938279
hg1838279
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv828212
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564888
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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