A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690882



Internal ID18642477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:144970446..145072757hg38UCSC Ensembl
Innerchr8:146195832..146298143hg19UCSC Ensembl
Innerchr8:146166636..146268947hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38102312
hg19102312
hg18102312
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029382
Supporting Variants
Samples
Known GenesC8orf33, TMED10P1, ZNF252P, 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)nssv3690882
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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