A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155329



Internal ID22085834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:60519407..60537315hg38UCSC Ensembl
Outerchr16:60514913..60540490hg38UCSC Ensembl
Innerchr16:60553311..60571219hg19UCSC Ensembl
Outerchr16:60548817..60574394hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3825578
hg1925578
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4008817
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155329
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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