A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3650478



Internal ID18948759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257341..294462hg38UCSC Ensembl
Innerchr6:257341..294462hg19UCSC Ensembl
Innerchr6:202341..239462hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3837122
hg1937122
hg1837122
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024786
Supporting Variants
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)nssv3650478
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