A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv833728



Internal ID16127684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101700166..101713702hg38UCSC Ensembl
Innerchr14:102166503..102180039hg19UCSC Ensembl
Innerchr14:101236256..101249792hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3813537
hg1913537
hg1813537
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565884
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)nssv833728
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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