A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022399



Internal ID19111617
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 StatusM
Merged Variantsdgv7340n100
Supporting Variantsnssv3690895
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)nsv1022399
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer