A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3521522



Internal ID18473117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:103385173..103447905hg38UCSC Ensembl
Innerchr10:105144930..105207662hg19UCSC Ensembl
Innerchr10:105134920..105197652hg18UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3862733
hg1962733
hg1862733
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053123
Supporting Variants
Samples
Known GenesCALHM2, MIR1307, PDCD11, TAF5, USMG5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3521522
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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