A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039039



Internal ID18781570
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 StatusM
Merged Variantsdgv1971n100
Supporting Variantsnssv3533452
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)nsv1039039
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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