A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5576646



Internal ID21525087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154744623..154744937hg38UCSC Ensembl
chr5:154124183..154124497hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133075
SamplesNA24385
Known GenesLARP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5576646
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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