A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3506536



Internal ID18804817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:130185092..130209034hg38UCSC Ensembl
Innerchr10:131983356..132007298hg19UCSC Ensembl
Innerchr10:131873346..131897288hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3823943
hg1923943
hg1823943
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042264
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3506536
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