A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022662



Internal ID19111880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:349386..361143hg38UCSC Ensembl
Innerchr6:349386..361143hg19UCSC Ensembl
Innerchr6:294386..306143hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3811758
hg1911758
hg1811758
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5903n100
Supporting Variantsnssv3654654
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)nsv1022662
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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