A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033904



Internal ID19123126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:20127365..20210143hg38UCSC Ensembl
Innerchr6:20127596..20210374hg19UCSC Ensembl
Innerchr6:20235575..20318353hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3882779
hg1982779
hg1882779
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654816
Samples
Known GenesMBOAT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033904
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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