A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584491



Internal ID21533032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:105822290..105824272hg38UCSC Ensembl
chr2:106438746..106440728hg19UCSC Ensembl
Cytoband2q12.2
Allele length
AssemblyAllele length
hg381983
hg191983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17107824
SamplesNA19238
Known GenesNCK2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584491
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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