A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv828213



Internal ID16122169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:62238616..62289015hg38UCSC Ensembl
Innerchr14:62705334..62755733hg19UCSC Ensembl
Innerchr14:61775087..61825486hg18UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3850400
hg1950400
hg1850400
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564889
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)nssv828213
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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