A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022298



Internal ID19111516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:137288604..137439330hg38UCSC Ensembl
Innerchr6:137609741..137760467hg19UCSC Ensembl
Innerchr6:137651434..137802160hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38150727
hg19150727
hg18150727
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654413
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)nsv1022298
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