A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572973



Internal ID21521369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62229964..62230290hg38UCSC Ensembl
chr2:62457099..62457425hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17113357
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572973
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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