A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv827229



Internal ID16121185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:42502585..42610170hg38UCSC Ensembl
Innerchr14:42971788..43079373hg19UCSC Ensembl
Innerchr14:42041538..42149123hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38107586
hg19107586
hg18107586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564571
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv827229
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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