A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031078



Internal ID19120299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:772699..861686hg38UCSC Ensembl
Innerchr8:722699..811686hg19UCSC Ensembl
Innerchr8:712699..801686hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3888988
hg1988988
hg1888988
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3675028
Samples
Known GenesERICH1-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031078
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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