A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033251



Internal ID18775785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:27217224..27249116hg38UCSC Ensembl
Innerchr8:27074741..27106633hg19UCSC Ensembl
Innerchr8:27130658..27162550hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3831893
hg1931893
hg1831893
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3685518
Samples
Known GenesSTMN4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033251
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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