A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876586



Internal ID22651547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156132821..156133758hg38UCSC Ensembl
chr1:156102612..156103549hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38938
hg19938
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355152
Samples
Known GenesLMNA, MIR7851
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876586
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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