A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579192



Internal ID21527668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:239035990..239036129hg38UCSC Ensembl
chr2:239957686..239957825hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17112391
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579192
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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