A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020902



Internal ID18763436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:73413975..73464215hg38UCSC Ensembl
Innerchr8:74326210..74376450hg19UCSC Ensembl
Innerchr8:74488764..74539004hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3850241
hg1950241
hg1850241
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689560
Samples
Known GenesSTAU2, STAU2-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020902
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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