A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042982



Internal ID18785513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46174643..46286428hg38UCSC Ensembl
Innerchr10:47545879..47657664hg19UCSC Ensembl
Innerchr10:47015885..47127670hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38111786
hg19111786
hg18111786
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv831n100
Supporting Variantsnssv3514644
Samples
Known GenesANTXRLP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042982
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