A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886999



Internal ID22661989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:226867189..226868497hg38UCSC Ensembl
chr1:227054890..227056198hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg381309
hg191309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353867
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886999
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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