A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027533



Internal ID19116752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:285695..382559hg38UCSC Ensembl
Innerchr6:285695..382559hg19UCSC Ensembl
Innerchr6:230695..327559hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3896865
hg1996865
hg1896865
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5887n100
Supporting Variantsnssv3747810
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)nsv1027533
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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