A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900826



Internal ID22675973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:150292690..150355306hg38UCSC Ensembl
chr2:151149204..151211820hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg3862617
hg1962617
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17408195
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900826
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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