A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896413



Internal ID22671506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:234655060..234663426hg38UCSC Ensembl
chr2:235563704..235572070hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg388367
hg198367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402298
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896413
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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