A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654471



Internal ID18952752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:150925524..150946575hg38UCSC Ensembl
Innerchr6:151246660..151267711hg19UCSC Ensembl
Innerchr6:151288353..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 StatusS
Merged Variantsnsv1020201
Supporting Variants
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)nssv3654471
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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