A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517327



Internal ID15444620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:29160496..29195836hg38UCSC Ensembl
Innerchr11:29182043..29217383hg19UCSC Ensembl
Innerchr11:29138619..29173959hg18UCSC Ensembl
Innerchr11:29138619..29173959hg17UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3835341
hg1935341
hg1835341
hg1735341
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv656027, nssv677832, nssv666147, nssv663145, nssv682015, nssv651727, nssv655624, nssv677051, nssv687240
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517327
Frequency
Sample Size2026
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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