A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516622



Internal ID15097229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1927731..1993479hg38UCSC Ensembl
Innerchr11:1948961..2014709hg19UCSC Ensembl
Innerchr11:1905537..1971285hg18UCSC Ensembl
Innerchr11:1905537..1971285hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3865749
hg1965749
hg1865749
hg1765749
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697756, nssv669619, nssv680624
Samples
Known GenesMRPL23, MRPL23-AS1, TNNT3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516622
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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