A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038324



Internal ID18780855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:42709000..42808429hg38UCSC Ensembl
Innerchr14:43178203..43277632hg19UCSC Ensembl
Innerchr14:42247953..42347382hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3899430
hg1999430
hg1899430
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3712304
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038324
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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