A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045115



Internal ID18787646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:17037131..17167193hg38UCSC Ensembl
Innerchr10:17079130..17209192hg19UCSC Ensembl
Innerchr10:17119136..17249198hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38130063
hg19130063
hg18130063
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3519974, nssv3515398
Samples
Known GenesCUBN, TRDMT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045115
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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