A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3506391



Internal ID18804672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:24088733..24107259hg38UCSC Ensembl
Innerchr10:24377662..24396188hg19UCSC Ensembl
Innerchr10:24417668..24436194hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3818527
hg1918527
hg1818527
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047756
Supporting Variants
Samples
Known GenesKIAA1217
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3506391
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