A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5577001



Internal ID21525447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146412871..146413845hg38UCSC Ensembl
chr5:145792434..145793408hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38975
hg19975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128417
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5577001
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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