A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020641



Internal ID19109860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257341..361143hg38UCSC Ensembl
Innerchr6:257341..361143hg19UCSC Ensembl
Innerchr6:202341..306143hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38103803
hg19103803
hg18103803
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5880n100
Supporting Variantsnssv3651647, nssv3651641, nssv3651645, nssv3651635, nssv3651644, nssv3651650, nssv3651648, nssv3651646, nssv3651642, nssv3651638, nssv3651634, nssv3651633, nssv3651640, nssv3651636, nssv3651649, nssv3651639, nssv3651637, nssv3651643
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)nsv1020641
Frequency
Sample Size11257
Observed Gain15
Observed Loss3
Observed Complex0
Frequencyn/a


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