A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025559



Internal ID19114777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:253861..294825hg38UCSC Ensembl
Innerchr6:253861..294825hg19UCSC Ensembl
Innerchr6:198861..239825hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3840965
hg1940965
hg1840965
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5881n100
Supporting Variantsnssv3650411, nssv3746769, nssv3650409, nssv3650410
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)nsv1025559
Frequency
Sample Size11257
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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