A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024004



Internal ID19113221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:36397614..36484141hg38UCSC Ensembl
Innerchr8:36255132..36341659hg19UCSC Ensembl
Innerchr8:36374690..36460817hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3886528
hg1986528
hg1886128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3685564, nssv3685565
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024004
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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