A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521884



Internal ID15102491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:135433333..135504563hg38UCSC Ensembl
Innerchr6:135754471..135825701hg19UCSC Ensembl
Innerchr6:135796164..135867394hg18UCSC Ensembl
Innerchr6:135796164..135867394hg17UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3871231
hg1971231
hg1871231
hg1771231
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694656
Samples
Known GenesAHI1, LINC00271, MIR548H4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521884
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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