A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029666



Internal ID18772197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:142272962..142321947hg38UCSC Ensembl
Innerchr6:142594099..142643084hg19UCSC Ensembl
Innerchr6:142635792..142684777hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3848986
hg1948986
hg1848986
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749555
Samples
Known GenesGPR126
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029666
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer