A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584301



Internal ID21532838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:100777355..100777427hg38UCSC Ensembl
chr2:101393817..101393889hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17107434
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584301
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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