A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572965



Internal ID21521361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24774239..24774292hg38UCSC Ensembl
chr7:24813858..24813911hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144922
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572965
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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