A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519167



Internal ID15099774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:135433333..135452087hg38UCSC Ensembl
Innerchr6:135754471..135773225hg19UCSC Ensembl
Innerchr6:135796164..135814918hg18UCSC Ensembl
Innerchr6:135796164..135814918hg17UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3818755
hg1918755
hg1818755
hg1718755
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694312
Samples
Known GenesAHI1, MIR548H4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519167
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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