A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036315



Internal ID19125534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100915376..100965338hg38UCSC Ensembl
Innerchr14:101381713..101431675hg19UCSC Ensembl
Innerchr14:100451466..100501428hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3849963
hg1949963
hg1849963
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1970n100
Supporting Variantsnssv3533456, nssv3533455
Samples
Known GenesSNORD113-1, SNORD113-2, SNORD113-3, SNORD113-4, SNORD113-5, SNORD113-6, SNORD113-7, SNORD113-8, SNORD113-9, SNORD114-1, SNORD114-2, SNORD114-3, SNORD114-4, SNORD114-5, SNORD114-6, SNORD114-7, SNORD114-8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036315
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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