A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565454



Internal ID16352863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:85982294..86024268hg38UCSC Ensembl
Innerchr14:86448638..86490612hg19UCSC Ensembl
Innerchr14:85518391..85560365hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3841975
hg1941975
hg1841975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3832n54
Supporting Variantsnssv832010
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565454
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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