A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525308



Internal ID15105915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:15218358..15219878hg38UCSC Ensembl
Innerchr3:15259865..15261385hg19UCSC Ensembl
Innerchr3:15234869..15236389hg18UCSC Ensembl
Innerchr3:15234869..15236389hg17UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg381521
hg191521
hg181521
hg171521
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701415
Samples
Known GenesCAPN7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525308
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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