A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020124



Internal ID19109343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:260364..361143hg38UCSC Ensembl
Innerchr6:260364..361143hg19UCSC Ensembl
Innerchr6:205364..306143hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38100780
hg19100780
hg18100780
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5874n100
Supporting Variantsnssv3652749, nssv3652748
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)nsv1020124
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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