A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3512561



Internal ID18810842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:84002158..84016279hg38UCSC Ensembl
Innerchr10:85761914..85776035hg19UCSC Ensembl
Innerchr10:85751894..85766015hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3814122
hg1914122
hg1814122
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042775
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)nssv3512561
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