A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155358



Internal ID22085863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:78435272..78470339hg38UCSC Ensembl
Outerchr16:78432861..78472009hg38UCSC Ensembl
Innerchr16:78469169..78504236hg19UCSC Ensembl
Outerchr16:78466758..78505906hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3839149
hg1939149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv125n97
Supporting Variantsnssv4009951
Samples
Known GenesWWOX
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155358
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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