A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583031



Internal ID21531550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:36505307..36505560hg38UCSC Ensembl
chr2:36732450..36732703hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg38254
hg19254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17114050
SamplesNA19238
Known GenesCRIM1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583031
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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