A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705806



Internal ID15095772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:75271895..75357723hg38UCSC Ensembl
Innerchr11:74982939..75068767hg19UCSC Ensembl
Innerchr11:74660587..74746415hg18UCSC Ensembl
Innerchr11:74660587..74746415hg17UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3885829
hg1985829
hg1885829
hg1785829
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522447
Supporting Variants
Samples
Known GenesARRB1, MIR326
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705806
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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