A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022744



Internal ID19111962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:302294..378703hg38UCSC Ensembl
Innerchr6:302294..378703hg19UCSC Ensembl
Innerchr6:247294..323703hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3876410
hg1976410
hg1876410
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5892n100
Supporting Variantsnssv3747834
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)nsv1022744
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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