A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019014



Internal ID19108231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:264744..323084hg38UCSC Ensembl
Innerchr6:264744..323084hg19UCSC Ensembl
Innerchr6:209744..268084hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3858341
hg1958341
hg1858341
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5885n100
Supporting Variantsnssv3653557
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)nsv1019014
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