A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155819



Internal ID22086324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:43630029..43639979hg38UCSC Ensembl
Outerchr1:43626356..43645854hg38UCSC Ensembl
Innerchr1:44095700..44105650hg19UCSC Ensembl
Outerchr1:44092027..44111525hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg3819499
hg1919499
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4015235
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155819
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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