A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155854



Internal ID22086359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:119287958..119292266hg38UCSC Ensembl
Outerchr2:119287781..119293268hg38UCSC Ensembl
Innerchr2:120045534..120049842hg19UCSC Ensembl
Outerchr2:120045357..120050844hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg385488
hg195488
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4013299
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155854
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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