A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519594



Internal ID15100201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:7652157..7685084hg38UCSC Ensembl
Innerchr11:7673388..7706315hg19UCSC Ensembl
Innerchr11:7629964..7662891hg18UCSC Ensembl
Innerchr11:7629964..7662891hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3832928
hg1932928
hg1832928
hg1732928
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv58n21
Supporting Variantsnssv696941
Samples
Known GenesCYB5R2, PPFIBP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519594
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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