A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023071



Internal ID19112288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:290586..382897hg38UCSC Ensembl
Innerchr6:290586..382897hg19UCSC Ensembl
Innerchr6:235586..327897hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3892312
hg1992312
hg1892312
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5888n100
Supporting Variantsnssv3653700, nssv3653702, nssv3653701
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)nsv1023071
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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