A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053673



Internal ID18796204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105563288..106877229hg38UCSC Ensembl
Innerchr14:106029625..107285437hg19UCSC Ensembl
Innerchr14:105100670..106356482hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg381313942
hg191255813
hg181255813
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3529832, nssv3529833
Samples
Known GenesADAM6, ELK2AP, KIAA0125, LINC00221, LINC00226, MIR8071-1, MIR8071-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053673
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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