A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690895



Internal ID18989176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:144992870..145070157hg38UCSC Ensembl
Innerchr8:146218256..146295543hg19UCSC Ensembl
Innerchr8:146189060..146266347hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3877288
hg1977288
hg1877288
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022399
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)nssv3690895
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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