A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565378



Internal ID16352787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:84604267..84674640hg38UCSC Ensembl
Innerchr14:85070611..85140984hg19UCSC Ensembl
Innerchr14:84140364..84210737hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3870374
hg1970374
hg1870374
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv831395
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565378
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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