A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592033



Internal ID16032756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:150408383..150410440hg38UCSC Ensembl
Innerchr3:150126170..150128227hg19UCSC Ensembl
Innerchr3:151608860..151610917hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg382058
hg192058
hg182058
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8649n54
Supporting Variantsnssv976730
Samples
Known GenesTSC22D2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592033
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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