A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697756



Internal ID15434408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1980665..1988665hg38UCSC Ensembl
Innerchr11:2001895..2009895hg19UCSC Ensembl
Innerchr11:1958471..1966471hg18UCSC Ensembl
Innerchr11:1958471..1966471hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg388001
hg198001
hg188001
hg178001
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516622
Supporting Variants
Samples
Known GenesMRPL23-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697756
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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