A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565024



Internal ID16352433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:70221529..70222487hg38UCSC Ensembl
Innerchr14:70688246..70689204hg19UCSC Ensembl
Innerchr14:69757999..69758957hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38959
hg19959
hg18959
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3748n54
Supporting Variantsnssv828975, nssv828976
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565024
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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