A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020113



Internal ID19109332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:331800..361143hg38UCSC Ensembl
Innerchr6:331800..361143hg19UCSC Ensembl
Innerchr6:276800..306143hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3829344
hg1929344
hg1829344
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654628, nssv3654627, nssv3654631, nssv3654629, nssv3654630
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)nsv1020113
Frequency
Sample Size11257
Observed Gain2
Observed Loss3
Observed Complex0
Frequencyn/a


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