A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020571



Internal ID19109790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257341..351364hg38UCSC Ensembl
Innerchr6:257341..351364hg19UCSC Ensembl
Innerchr6:202341..296364hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3894024
hg1994024
hg1894024
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5874n100
Supporting Variantsnssv3651621, nssv3651622, nssv3651620
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)nsv1020571
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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