A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701052



Internal ID15091018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55674892..55716176hg38UCSC Ensembl
Innerchr11:55442368..55483652hg19UCSC Ensembl
Innerchr11:55198944..55240228hg18UCSC Ensembl
Innerchr11:55198944..55240228hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3841285
hg1941285
hg1841285
hg1741285
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517440
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701052
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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