A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021709



Internal ID19110927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:145005803..145072757hg38UCSC Ensembl
Innerchr8:146231189..146298143hg19UCSC Ensembl
Innerchr8:146201993..146268947hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3866955
hg1966955
hg1866955
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7341n100
Supporting Variantsnssv3690909, nssv3690910, nssv3690911
Samples
Known GenesC8orf33, ZNF252P-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021709
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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