A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565370



Internal ID16352779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:83380429..83425983hg38UCSC Ensembl
Innerchr14:83846773..83892327hg19UCSC Ensembl
Innerchr14:82916526..82962080hg18UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg3845555
hg1945555
hg1845555
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3817n54
Supporting Variantsnssv831386
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565370
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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