A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039520



Internal ID19128739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:45356841..45543637hg38UCSC Ensembl
Innerchr14:45826044..46012840hg19UCSC Ensembl
Innerchr14:44895794..45082590hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38186797
hg19186797
hg18186797
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1905n100
Supporting Variantsnssv3530454
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)nsv1039520
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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