A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021894



Internal ID19111112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:350190..361143hg38UCSC Ensembl
Innerchr6:350190..361143hg19UCSC Ensembl
Innerchr6:295190..306143hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3810954
hg1910954
hg1810954
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5903n100
Supporting Variantsnssv3654657
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)nsv1021894
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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