A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016490



Internal ID18759025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:32206493..32228652hg38UCSC Ensembl
Innerchr8:32064009..32086168hg19UCSC Ensembl
Innerchr8:32183551..32205710hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3822160
hg1922160
hg1822160
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3685557
Samples
Known GenesNRG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016490
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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