A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527886



Internal ID15455179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:103330047..104271049hg38UCSC Ensembl
Innerchr3:103048891..103989893hg19UCSC Ensembl
Innerchr3:104531581..105472583hg18UCSC Ensembl
Innerchr3:104531581..105472583hg17UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38941003
hg19941003
hg18941003
hg17941003
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704388
Samples
Known GenesMIR548A3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527886
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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