A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526786



Internal ID15454079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:37030699..37068147hg38UCSC Ensembl
Innerchr14:37499904..37537352hg19UCSC Ensembl
Innerchr14:36569655..36607103hg18UCSC Ensembl
Innerchr14:36569655..36607103hg17UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg3837449
hg1937449
hg1837449
hg1737449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703138
Samples
Known GenesSLC25A21
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526786
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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