A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051396



Internal ID18793927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:124738468..124800091hg38UCSC Ensembl
Innerchr10:126427037..126488660hg19UCSC Ensembl
Innerchr10:126417027..126478650hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3861624
hg1961624
hg1861624
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3519579
Samples
Known GenesFAM53B, METTL10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051396
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