A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052547



Internal ID19141766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112954828..113024761hg38UCSC Ensembl
Innerchr9:115717108..115787041hg19UCSC Ensembl
Innerchr9:114756929..114826862hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3869934
hg1969934
hg1869934
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7703n100
Supporting Variantsnssv3695107, nssv3695106
Samples
Known GenesZNF883
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052547
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