A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052158



Internal ID19141377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:128462679..128487672hg38UCSC Ensembl
Innerchr10:130260943..130285936hg19UCSC Ensembl
Innerchr10:130150933..130175926hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3824994
hg1924994
hg1824994
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3518985
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)nsv1052158
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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