A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045435



Internal ID18787966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:97822001..97855990hg38UCSC Ensembl
Innerchr10:99581758..99615747hg19UCSC Ensembl
Innerchr10:99571748..99605737hg18UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3833990
hg1933990
hg1833990
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3508230
Samples
Known GenesGOLGA7B, LINC00866
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045435
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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