A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565513



Internal ID16006236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:88945838..89018323hg38UCSC Ensembl
Innerchr14:89412182..89484667hg19UCSC Ensembl
Innerchr14:88481935..88554420hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3872486
hg1972486
hg1872486
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv832172
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565513
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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