A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526433



Internal ID15453726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:76565079..76802530hg38UCSC Ensembl
Innerchr1:77030764..77268215hg19UCSC Ensembl
Innerchr1:76803352..77040803hg18UCSC Ensembl
Innerchr1:76742785..76980236hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38237452
hg19237452
hg18237452
hg17237452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702736
Samples
Known GenesST6GALNAC3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526433
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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