A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6162n100



Internal ID22792249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150925524..150946575hg38UCSC Ensembl
chr6:151246660..151267711hg19UCSC Ensembl
chr6:151288353..151309404hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3821052
hg1921052
hg1821052
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033932, nsv1020201
Samples
Known GenesMTHFD1L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6162n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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