A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517429



Internal ID15444722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:34174937..34178302hg38UCSC Ensembl
Innerchr11:34196484..34199849hg19UCSC Ensembl
Innerchr11:34153060..34156425hg18UCSC Ensembl
Innerchr11:34153060..34156425hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg383366
hg193366
hg183366
hg173366
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv665303, nssv667767, nssv682079, nssv660240, nssv667868, nssv652757, nssv688737, nssv656071, nssv672505, nssv667359, nssv688065, nssv675826, nssv670875, nssv653953, nssv656242, nssv662727, nssv687773, nssv670360, nssv681272, nssv690493, nssv677938, nssv652320, nssv661975, nssv666277, nssv664626
Samples
Known GenesABTB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517429
Frequency
Sample Size2026
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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