A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046825



Internal ID18789356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:99861014..99912354hg38UCSC Ensembl
Innerchr10:101620771..101672111hg19UCSC Ensembl
Innerchr10:101610761..101662101hg18UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3851341
hg1951341
hg1851341
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3509277
Samples
Known GenesDNMBP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046825
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