A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525024



Internal ID15105631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86479615..86593836hg38UCSC Ensembl
Innerchr16:86513221..86627442hg19UCSC Ensembl
Innerchr16:85070722..85184943hg18UCSC Ensembl
Innerchr16:85070722..85184943hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38114222
hg19114222
hg18114222
hg17114222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701063
Samples
Known GenesFENDRR, FLJ30679, FOXC2, FOXF1, FOXL1, MTHFSD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525024
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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