A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898726



Internal ID22673846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:149568216..149568396hg38UCSC Ensembl
chr2:150424730..150424910hg19UCSC Ensembl
Cytoband2q23.2
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17407264
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898726
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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