A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043832



Internal ID18786363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26380111..26520471hg38UCSC Ensembl
Innerchr10:26669040..26809400hg19UCSC Ensembl
Innerchr10:26709046..26849406hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38140361
hg19140361
hg18140361
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3507382
Samples
Known GenesAPBB1IP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043832
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