A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033771



Internal ID19122992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:84785707..84808064hg38UCSC Ensembl
Innerchr8:85697942..85720299hg19UCSC Ensembl
Innerchr8:85860497..85882854hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3822358
hg1922358
hg1822358
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689644, nssv3689643
Samples
Known GenesRALYL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033771
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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