A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5577425



Internal ID21525878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:31441319..31441368hg38UCSC Ensembl
chr8:31298835..31298884hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153274
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5577425
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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