A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524478



Internal ID15105085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89139102..89168540hg38UCSC Ensembl
Innerchr16:89205510..89234948hg19UCSC Ensembl
Innerchr16:87733011..87762449hg18UCSC Ensembl
Innerchr16:87733011..87762449hg17UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3829439
hg1929439
hg1829439
hg1729439
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700416
Samples
Known GenesACSF3, LINC00304, LOC400558
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524478
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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