A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881186



Internal ID22656160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157946796..157947112hg38UCSC Ensembl
chr1:157916586..157916902hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368299
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881186
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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