A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3466893



Internal ID19062006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:76226372..76258967hg38UCSC Ensembl
Innerchr1:76692057..76724652hg19UCSC Ensembl
Innerchr1:76464645..76497240hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3832596
hg1932596
hg1832596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001452
Supporting Variants
Samples
Known GenesST6GALNAC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3466893
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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