A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155922



Internal ID22086427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:226481353..226489451hg38UCSC Ensembl
Outerchr2:226481318..226490315hg38UCSC Ensembl
Innerchr2:227346069..227354167hg19UCSC Ensembl
Outerchr2:227346034..227355031hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg388998
hg198998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016188
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155922
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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