A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654641



Internal ID18952922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:336797..385772hg38UCSC Ensembl
Innerchr6:336797..385772hg19UCSC Ensembl
Innerchr6:281797..330772hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3848976
hg1948976
hg1848976
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028112
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)nssv3654641
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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