A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032451



Internal ID18774985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:45935900..46831628hg38UCSC Ensembl
Innerchr8:46847522..47743250hg19UCSC Ensembl
Innerchr8:46966687..47862415hg18UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg38895729
hg19895729
hg18895729
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7202n100
Supporting Variantsnssv3687391, nssv3687386, nssv3687385, nssv3687387, nssv3687383, nssv3687389, nssv3687382, nssv3687384, nssv3687388, nssv3687390
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)nsv1032451
Frequency
Sample Size29084
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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