A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4009949



Internal ID22071580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:78432243..78470339hg38UCSC Ensembl
Outerchr16:78429900..78472009hg38UCSC Ensembl
Innerchr16:78466140..78504236hg19UCSC Ensembl
Outerchr16:78463797..78505906hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3842110
hg1942110
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155356
Supporting Variants
Samples
Known GenesWWOX
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4009949
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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