A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033571



Internal ID19122792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:260364..302294hg38UCSC Ensembl
Innerchr6:260364..302294hg19UCSC Ensembl
Innerchr6:205364..247294hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3841931
hg1941931
hg1841931
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5886n100
Supporting Variantsnssv3652738
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)nsv1033571
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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