A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5571584



Internal ID21519965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231464731..231465285hg38UCSC Ensembl
chr2:232329442..232329996hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38555
hg19555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17111802
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5571584
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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