A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028726



Internal ID18771257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:106804613..107380319hg38UCSC Ensembl
Innerchr8:107816841..108392547hg19UCSC Ensembl
Innerchr8:107886017..108461723hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38575707
hg19575707
hg18575707
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757334
Samples
Known GenesANGPT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028726
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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