A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582721



Internal ID21531236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:72087726..72087826hg38UCSC Ensembl
chr2:72314856..72314956hg19UCSC Ensembl
Cytoband2p13.2
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17115009
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582721
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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