A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528349



Internal ID15108956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:138306554..138413551hg38UCSC Ensembl
Innerchr3:138025396..138132393hg19UCSC Ensembl
Innerchr3:139508086..139615083hg18UCSC Ensembl
Innerchr3:139508094..139615091hg17UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38106998
hg19106998
hg18106998
hg17106998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704933
Samples
Known GenesMRAS, NME9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528349
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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