A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691711



Internal ID15081677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134288851..134346971hg38UCSC Ensembl
Innerchr11:134158745..134216865hg19UCSC Ensembl
Innerchr11:133663955..133722075hg18UCSC Ensembl
Innerchr11:133663955..133722075hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3858121
hg1958121
hg1858121
hg1758121
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516459
Supporting Variants
Samples
Known GenesGLB1L2, GLB1L3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691711
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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