A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051052



Internal ID19140271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:80381895..80415193hg38UCSC Ensembl
Innerchr10:82141651..82174949hg19UCSC Ensembl
Innerchr10:82131631..82164929hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3833299
hg1933299
hg1833299
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3513508
Samples
Known GenesFAM213A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051052
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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