A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901327



Internal ID22676477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:228894572..228895190hg38UCSC Ensembl
chr2:229759288..229759906hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg38619
hg19619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399991
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901327
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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