A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567394



Internal ID21515729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:163008365..163008679hg38UCSC Ensembl
chr5:162435371..162435685hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124240
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5567394
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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