A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594934



Internal ID16382343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:97676842..97827148hg38UCSC Ensembl
Innerchr4:98597993..98748299hg19UCSC Ensembl
Innerchr4:98817016..98967322hg18UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38150307
hg19150307
hg18150307
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9179n54
Supporting Variantsnssv1003432
Samples
Known GenesSTPG2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594934
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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