A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4010486



Internal ID22072117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:9590855..9688279hg38UCSC Ensembl
Outerchr16:9584382..9689281hg38UCSC Ensembl
Innerchr16:9684712..9782136hg19UCSC Ensembl
Outerchr16:9678239..9783138hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38104900
hg19104900
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155228
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4010486
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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