A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032899



Internal ID19122121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:20170195..20197650hg38UCSC Ensembl
Innerchr6:20170426..20197881hg19UCSC Ensembl
Innerchr6:20278405..20305860hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3827456
hg1927456
hg1827456
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654817
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)nsv1032899
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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