A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5576613



Internal ID21525054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6396901..6396959hg38UCSC Ensembl
chr5:6397014..6397072hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17154775
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5576613
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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