A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3747733



Internal ID19046014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257341..384097hg38UCSC Ensembl
Innerchr6:257341..384097hg19UCSC Ensembl
Innerchr6:202341..329097hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38126757
hg19126757
hg18126757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025122
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)nssv3747733
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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