A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515786



Internal ID15442843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:166879286..166910565hg38UCSC Ensembl
Innerchr3:166597074..166628353hg19UCSC Ensembl
Innerchr3:168079768..168111047hg18UCSC Ensembl
Innerchr3:168079776..168111055hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3831280
hg1931280
hg1831280
hg1731280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664781, nssv687452
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515786
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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