A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903565



Internal ID22678734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:149513120..149518311hg38UCSC Ensembl
chr2:150369634..150374825hg19UCSC Ensembl
Cytoband2q23.2
Allele length
AssemblyAllele length
hg385192
hg195192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399631
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903565
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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