A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017047



Internal ID19106264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257341..378703hg38UCSC Ensembl
Innerchr6:257341..378703hg19UCSC Ensembl
Innerchr6:202341..323703hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38121363
hg19121363
hg18121363
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5878n100
Supporting Variantsnssv3652428, nssv3652427, nssv3652426, nssv3652429
Samples
Known GenesDUSP22
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017047
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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