A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610880



Internal ID16051603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:32136294..32370410hg38UCSC Ensembl
Innerchr8:31993810..32227926hg19UCSC Ensembl
Innerchr8:32113352..32347468hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38234117
hg19234117
hg18234117
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156829
SamplesHGDP00654
Known GenesNRG1, NRG1-IT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610880
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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