A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567602



Internal ID21515940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:156720350..156720400hg38UCSC Ensembl
chr2:157576862..157576912hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17109405
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5567602
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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