A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570394



Internal ID16011117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90307141..90396827hg38UCSC Ensembl
Innerchr15:90850373..90940059hg19UCSC Ensembl
Innerchr15:88651377..88741063hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3889687
hg1989687
hg1889687
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv848207
Samples
Known GenesGABARAPL3, IQGAP1, ZNF774
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570394
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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