A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3506529



Internal ID18804810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:24557774..24574091hg38UCSC Ensembl
Innerchr10:24846703..24863020hg19UCSC Ensembl
Innerchr10:24886709..24903026hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3816318
hg1916318
hg1816318
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042256
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)nssv3506529
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