A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3687241



Internal ID18985522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:40327353..40344169hg38UCSC Ensembl
Innerchr8:40184872..40201688hg19UCSC Ensembl
Innerchr8:40304029..40320845hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3816817
hg1916817
hg1816817
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020785
Supporting Variants
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)nssv3687241
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