A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834338



Internal ID16128294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103520119..103522107hg38UCSC Ensembl
Innerchr14:103986456..103988444hg19UCSC Ensembl
Innerchr14:103056209..103058197hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg381989
hg191989
hg181989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565988
Supporting Variants
Samples
Known GenesCKB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv834338
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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