A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517300



Internal ID15444593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:114600354..114641905hg38UCSC Ensembl
Innerchr11:114471076..114512627hg19UCSC Ensembl
Innerchr11:113976286..114017837hg18UCSC Ensembl
Innerchr11:113976286..114017837hg17UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3841552
hg1941552
hg1841552
hg1741552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv671959, nssv659240, nssv686287, nssv678684, nssv681245, nssv685237, nssv654251
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517300
Frequency
Sample Size2026
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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