A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526665



Internal ID15107272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:102363085..102397954hg38UCSC Ensembl
Innerchr10:104122842..104157711hg19UCSC Ensembl
Innerchr10:104112832..104147701hg18UCSC Ensembl
Innerchr10:104112832..104147701hg17UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3834870
hg1934870
hg1834870
hg1734870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702994
Samples
Known GenesGBF1, NFKB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526665
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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