A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3652680



Internal ID18950961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:258253..294825hg38UCSC Ensembl
Innerchr6:258253..294825hg19UCSC Ensembl
Innerchr6:203253..239825hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3836573
hg1936573
hg1836573
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016091
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)nssv3652680
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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