A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3747802



Internal ID19046083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:271761..381137hg38UCSC Ensembl
Innerchr6:271761..381137hg19UCSC Ensembl
Innerchr6:216761..326137hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38109377
hg19109377
hg18109377
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018436
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)nssv3747802
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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