A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029609



Internal ID18772140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:5187399..5397021hg38UCSC Ensembl
Innerchr6:5187633..5397254hg19UCSC Ensembl
Innerchr6:5132632..5342253hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38209623
hg19209622
hg18209622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5912n100
Supporting Variantsnssv3747908
Samples
Known GenesFARS2, LYRM4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029609
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