A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516354



Internal ID15443647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:64038696..64073143hg38UCSC Ensembl
Innerchr16:64072600..64107047hg19UCSC Ensembl
Innerchr16:62630101..62664548hg18UCSC Ensembl
Innerchr16:62630101..62664548hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3834448
hg1934448
hg1834448
hg1734448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv690039, nssv694162, nssv685455, nssv684224, nssv680262, nssv686763, nssv684047, nssv661877, nssv667746, nssv676176, nssv674557, nssv677672, nssv684438, nssv655097, nssv682059, nssv682288, nssv689577, nssv659776
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516354
Frequency
Sample Size2026
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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