A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv975060



Internal ID16269016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:141219704..141286732hg38UCSC Ensembl
Innerchr3:140938546..141005574hg19UCSC Ensembl
Innerchr3:142421236..142488264hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3867029
hg1967029
hg1867029
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591892
Supporting Variants
Samples
Known GenesACPL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv975060
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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