A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025121



Internal ID19114339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:257341..373441hg38UCSC Ensembl
Innerchr6:257341..373441hg19UCSC Ensembl
Innerchr6:202341..318441hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38116101
hg19116101
hg18116101
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5880n100
Supporting Variantsnssv3652404, nssv3652405, nssv3652406, nssv3652409, nssv3652408, nssv3652407
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)nsv1025121
Frequency
Sample Size11257
Observed Gain1
Observed Loss5
Observed Complex0
Frequencyn/a


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