A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020094



Internal ID19109313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:314950..373441hg38UCSC Ensembl
Innerchr6:314950..373441hg19UCSC Ensembl
Innerchr6:259950..318441hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3858492
hg1958492
hg1858492
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5894n100
Supporting Variantsnssv3653831
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)nsv1020094
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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