A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027489



Internal ID18770021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:142015585..142108766hg38UCSC Ensembl
Innerchr6:142336722..142429903hg19UCSC Ensembl
Innerchr6:142378415..142471596hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3893182
hg1993182
hg1893182
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654449
Samples
Known GenesNMBR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027489
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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