A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565433



Internal ID16352842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:85816380..85844064hg38UCSC Ensembl
Innerchr14:86282724..86310408hg19UCSC Ensembl
Innerchr14:85352477..85380161hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3827685
hg1927685
hg1827685
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3825n54
Supporting Variantsnssv831947
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565433
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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