A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565451



Internal ID16352860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:85960618..86020992hg38UCSC Ensembl
Innerchr14:86426962..86487336hg19UCSC Ensembl
Innerchr14:85496715..85557089hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3860375
hg1960375
hg1860375
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3831n54
Supporting Variantsnssv832005
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565451
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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