A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701678



Internal ID15438330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:284613..344878hg38UCSC Ensembl
Innerchr6:284613..344878hg19UCSC Ensembl
Innerchr6:229613..289878hg18UCSC Ensembl
Innerchr6:229613..289878hg17UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3860266
hg1960266
hg1860266
hg1760266
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525541
Supporting Variants
Samples
Known GenesDUSP22
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701678
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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