A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572697



Internal ID21521089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:24308346..24313450hg38UCSC Ensembl
chr5:24308455..24313559hg19UCSC Ensembl
Cytoband5p14.2
Allele length
AssemblyAllele length
hg385105
hg195105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17137874
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572697
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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