A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015215



Internal ID19104432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:134666325..134688161hg38UCSC Ensembl
Innerchr6:134987463..135009299hg19UCSC Ensembl
Innerchr6:135029156..135050992hg18UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3821837
hg1921837
hg1821837
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654401
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)nsv1015215
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