A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516876



Internal ID15097483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3680577..3697203hg38UCSC Ensembl
Innerchr16:3730578..3747204hg19UCSC Ensembl
Innerchr16:3670579..3687205hg18UCSC Ensembl
Innerchr16:3670579..3687205hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3816627
hg1916627
hg1816627
hg1716627
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv654623, nssv673049
Samples
Known GenesTRAP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516876
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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