A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3747793



Internal ID19046074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:264744..382559hg38UCSC Ensembl
Innerchr6:264744..382559hg19UCSC Ensembl
Innerchr6:209744..327559hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38117816
hg19117816
hg18117816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022899
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)nssv3747793
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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