A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3533452



Internal ID18485047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100910441..100973221hg38UCSC Ensembl
Innerchr14:101376778..101439558hg19UCSC Ensembl
Innerchr14:100446531..100509311hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3862781
hg1962781
hg1862781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039039
Supporting Variants
Samples
Known GenesSNORD113-1, SNORD113-2, SNORD113-3, SNORD113-4, SNORD113-5, SNORD113-6, SNORD113-7, SNORD113-8, SNORD113-9, SNORD114-1, SNORD114-10, SNORD114-11, SNORD114-12, SNORD114-13, SNORD114-14, SNORD114-15, SNORD114-2, SNORD114-3, SNORD114-4, SNORD114-5, SNORD114-6, SNORD114-7, SNORD114-8, SNORD114-9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3533452
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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