A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657093



Internal ID15393745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134525348..134783934hg38UCSC Ensembl
Innerchr11:134395242..134653828hg19UCSC Ensembl
Innerchr11:133900452..134159038hg18UCSC Ensembl
Innerchr11:133900452..134159038hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38258587
hg19258587
hg18258587
hg17258587
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517742
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657093
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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