A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565429



Internal ID16352838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:85813241..85843820hg38UCSC Ensembl
Innerchr14:86279585..86310164hg19UCSC Ensembl
Innerchr14:85349338..85379917hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3830580
hg1930580
hg1830580
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3825n54
Supporting Variantsnssv831942, nssv831943
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565429
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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