A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051283



Internal ID18793814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5463511..5577978hg38UCSC Ensembl
Innerchr10:5505474..5619941hg19UCSC Ensembl
Innerchr10:5495474..5609941hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38114468
hg19114468
hg18114468
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3492958
Samples
Known GenesCALML3, CALML5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051283
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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