A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654654



Internal ID18952935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:349386..361143hg38UCSC Ensembl
Innerchr6:349386..361143hg19UCSC Ensembl
Innerchr6:294386..306143hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3811758
hg1911758
hg1811758
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022662
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)nssv3654654
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