A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593093



Internal ID16380502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:196968637..196969752hg38UCSC Ensembl
Innerchr3:196695508..196696623hg19UCSC Ensembl
Innerchr3:198179905..198181020hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381116
hg191116
hg181116
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8852n54
Supporting Variantsnssv986964, nssv986965, nssv986966
Samples
Known GenesPIGZ
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593093
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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