A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1047572



Internal ID15900758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:295956..383546hg38UCSC Ensembl
Innerchr6:295956..383546hg19UCSC Ensembl
Innerchr6:240956..328546hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3887591
hg1987591
hg1887591
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600764
Supporting Variants
Samples
Known GenesDUSP22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1047572
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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