A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029662



Internal ID18772193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:108423086..108486537hg38UCSC Ensembl
Innerchr8:109435315..109498766hg19UCSC Ensembl
Innerchr8:109504491..109567942hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3863452
hg1963452
hg1863452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691270
Samples
Known GenesEMC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029662
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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