A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015482



Internal ID19104699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:73702312..73731445hg38UCSC Ensembl
Innerchr8:74614547..74643680hg19UCSC Ensembl
Innerchr8:74777101..74806234hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3829134
hg1929134
hg1829134
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689563
Samples
Known GenesSTAU2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015482
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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