A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655853



Internal ID15392505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:96475095..96534359hg38UCSC Ensembl
Innerchr11:96208259..96267523hg19UCSC Ensembl
Innerchr11:95847907..95907171hg18UCSC Ensembl
Innerchr11:95847907..95907171hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3859265
hg1959265
hg1859265
hg1759265
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516287
Supporting Variants
Samples
Known GenesJRKL-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv655853
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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