A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017984



Internal ID19107201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:285695..378703hg38UCSC Ensembl
Innerchr6:285695..378703hg19UCSC Ensembl
Innerchr6:230695..323703hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3893009
hg1993009
hg1893009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5888n100
Supporting Variantsnssv3653676
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)nsv1017984
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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