A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518529



Internal ID15445822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:150980815..150994105hg38UCSC Ensembl
Innerchr6:151301951..151315241hg19UCSC Ensembl
Innerchr6:151343644..151356934hg18UCSC Ensembl
Innerchr6:151394065..151407355hg17UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3813291
hg1913291
hg1813291
hg1713291
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695972
Samples
Known GenesMTHFD1L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518529
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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