A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690908



Internal ID18989189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:144995334..145072757hg38UCSC Ensembl
Innerchr8:146220720..146298143hg19UCSC Ensembl
Innerchr8:146191524..146268947hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3877424
hg1977424
hg1877424
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021946
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)nssv3690908
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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