A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525726



Internal ID15106333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11700211..11728210hg38UCSC Ensembl
Innerchr16:11794067..11822066hg19UCSC Ensembl
Innerchr16:11701568..11729567hg18UCSC Ensembl
Innerchr16:11701568..11729567hg17UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3828000
hg1928000
hg1828000
hg1728000
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701890
Samples
Known GenesTXNDC11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525726
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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