A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564475



Internal ID16351884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:41132802..41200899hg38UCSC Ensembl
Innerchr14:41602007..41670102hg19UCSC Ensembl
Innerchr14:40671757..40739852hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3868098
hg1968096
hg1868096
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3659n54
Supporting Variantsnssv826680, nssv826683, nssv826682, nssv826681
Samples
Known GenesLOC644919
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564475
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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