A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv826035



Internal ID16119991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:39998545..40103037hg38UCSC Ensembl
Innerchr14:40467749..40572241hg19UCSC Ensembl
Innerchr14:39537500..39641992hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38104493
hg19104493
hg18104493
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564421
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)nssv826035
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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