A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5452588



Internal ID230736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:181491256..181491559hg38UCSC Ensembl
chr2:182355983..182356286hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16927417
Samples
Known GenesITGA4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5452588
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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