A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023345



Internal ID18765878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:135556122..135930860hg38UCSC Ensembl
Innerchr6:135877260..136251998hg19UCSC Ensembl
Innerchr6:135918953..136293691hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38374739
hg19374739
hg18374739
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654406
Samples
Known GenesLINC00271, MIR548H4, PDE7B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023345
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