A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565892



Internal ID16353301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101707701..101713069hg38UCSC Ensembl
Innerchr14:102174038..102179406hg19UCSC Ensembl
Innerchr14:101243791..101249159hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg385369
hg195369
hg185369
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3923n54
Supporting Variantsnssv833743, nssv833744, nssv833742
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565892
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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