A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053862



Internal ID19143081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121676883..121701392hg38UCSC Ensembl
Innerchr10:123436397..123460906hg19UCSC Ensembl
Innerchr10:123426387..123450896hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3824510
hg1924510
hg1824510
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv985n100
Supporting Variantsnssv3520314
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)nsv1053862
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