A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3675028



Internal ID18973309
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 StatusS
Merged Variantsnsv1031078
Supporting Variants
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)nssv3675028
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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