A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5891136



Internal ID22666170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:171257301..171257480hg38UCSC Ensembl
chr2:172113811..172113990hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409468
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5891136
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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