A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155413



Internal ID22085918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:35772407..35864863hg38UCSC Ensembl
Outerchr2:35762881..35866763hg38UCSC Ensembl
Innerchr2:35997473..36089929hg19UCSC Ensembl
Outerchr2:35987947..36091829hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38103883
hg19103883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011178
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155413
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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