A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520248



Internal ID15447541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8942772..8943391hg38UCSC Ensembl
Innerchr11:8964319..8964938hg19UCSC Ensembl
Innerchr11:8920895..8921514hg18UCSC Ensembl
Innerchr11:8920895..8921514hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38620
hg19620
hg18620
hg17620
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv662104, nssv690673, nssv677958
Samples
Known GenesASCL3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520248
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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