A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3502158



Internal ID18800439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26861..97603hg38UCSC Ensembl
Innerchr10:72797..143543hg19UCSC Ensembl
Innerchr10:62797..133543hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3870743
hg1970747
hg1870747
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050135
Supporting Variants
Samples
Known GenesTUBB8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3502158
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