A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565446



Internal ID16352855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:85822569..85855940hg38UCSC Ensembl
Innerchr14:86288913..86322284hg19UCSC Ensembl
Innerchr14:85358666..85392037hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3833372
hg1933372
hg1833372
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3826n54
Supporting Variantsnssv831996, nssv831995
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565446
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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