A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3533517



Internal ID18485112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100918430..100982495hg38UCSC Ensembl
Innerchr14:101384767..101448832hg19UCSC Ensembl
Innerchr14:100454520..100518585hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3864066
hg1964066
hg1864066
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049435
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, SNORD114-16, SNORD114-17, SNORD114-18, SNORD114-19, SNORD114-2, SNORD114-20, SNORD114-21, 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)nssv3533517
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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