A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036343



Internal ID18778874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:21988852..22509792hg38UCSC Ensembl
Innerchr14:22457092..22978775hg19UCSC Ensembl
Innerchr14:21526932..22048615hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38520941
hg19521684
hg18521684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1803n100
Supporting Variantsnssv3712159
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)nsv1036343
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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