A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025932



Internal ID19115149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:265101..376925hg38UCSC Ensembl
Innerchr6:265101..376925hg19UCSC Ensembl
Innerchr6:210101..321925hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38111825
hg19111825
hg18111825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5878n100
Supporting Variantsnssv3653620
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)nsv1025932
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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