A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1975n100



Internal ID19012343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100925527..101000625hg38UCSC Ensembl
chr14:101391864..101466962hg19UCSC Ensembl
chr14:100461617..100536715hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3875099
hg1975099
hg1875099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043279, nsv1042697, nsv1048848, nsv1041318, nsv1042353, nsv1048662, nsv1043390
Samples
Known GenesSNORD113-2, 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, SNORD114-22, SNORD114-23, SNORD114-24, SNORD114-25, SNORD114-26, SNORD114-27, SNORD114-28, SNORD114-29, SNORD114-3, SNORD114-30, SNORD114-31, 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)dgv1975n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer