A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526347



Internal ID15106954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89905937..89913086hg38UCSC Ensembl
Innerchr16:89972345..89979494hg19UCSC Ensembl
Innerchr16:88499846..88506995hg18UCSC Ensembl
Innerchr16:88499846..88506995hg17UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg387150
hg197150
hg187150
hg177150
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702639
Samples
Known GenesTCF25
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526347
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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