A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049523



Internal ID18792054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5500146..5577978hg38UCSC Ensembl
Innerchr10:5542109..5619941hg19UCSC Ensembl
Innerchr10:5532109..5609941hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3877833
hg1977833
hg1877833
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv664n100
Supporting Variantsnssv3496706, nssv3500534
Samples
Known GenesCALML3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049523
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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