A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1047557



Internal ID15554057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:175522..311938hg38UCSC Ensembl
Innerchr6:175522..311938hg19UCSC Ensembl
Innerchr6:120522..256938hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38136417
hg19136417
hg18136417
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600740
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)nssv1047557
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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