A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1971n100



Internal ID19012339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100910441..100973221hg38UCSC Ensembl
chr14:101376778..101439558hg19UCSC Ensembl
chr14:100446531..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 StatusM
Merged Variants
Supporting Variantsnsv1039039, nsv1046601, nsv1050820
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)dgv1971n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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