A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524676



Internal ID15105283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11475598..11701723hg38UCSC Ensembl
Innerchr16:11569454..11795579hg19UCSC Ensembl
Innerchr16:11476955..11703080hg18UCSC Ensembl
Innerchr16:11476955..11703080hg17UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38226126
hg19226126
hg18226126
hg17226126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700647
Samples
Known GenesLITAF, SNN, TXNDC11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524676
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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