A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028547



Internal ID19117765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257341..355524hg38UCSC Ensembl
Innerchr6:257341..355524hg19UCSC Ensembl
Innerchr6:202341..300524hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3898184
hg1998184
hg1898184
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5880n100
Supporting Variantsnssv3651624, nssv3651626, nssv3651625
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)nsv1028547
Frequency
Sample Size11257
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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