A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008578



Internal ID19097795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:140188330..140223611hg38UCSC Ensembl
Innerchr3:139907172..139942453hg19UCSC Ensembl
Innerchr3:141389862..141425143hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3835282
hg1935282
hg1835282
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4909n100
Supporting Variantsnssv3608339
Samples
Known GenesCLSTN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008578
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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