A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052074



Internal ID19141293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:107361674..107372782hg38UCSC Ensembl
Innerchr10:109121432..109132540hg19UCSC Ensembl
Innerchr10:109111422..109122530hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3811109
hg1911109
hg1811109
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3514594, nssv3520597
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052074
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