A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028894



Internal ID19118113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16152658..16245245hg38UCSC Ensembl
Innerchr8:16010167..16102754hg19UCSC Ensembl
Innerchr8:16054538..16147125hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3892588
hg1992588
hg1892588
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3675958
Samples
Known GenesMSR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028894
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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