A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047756



Internal ID19136975
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 StatusM
Merged Variantsdgv691n100
Supporting Variantsnssv3506391, nssv3504447
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)nsv1047756
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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