A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015407



Internal ID19104624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:314950..364575hg38UCSC Ensembl
Innerchr6:314950..364575hg19UCSC Ensembl
Innerchr6:259950..309575hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3849626
hg1949626
hg1849626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5894n100
Supporting Variantsnssv3653828, nssv3653829
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)nsv1015407
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