A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5624800



Internal ID21573105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55006633..55006633hg38UCSC Ensembl
chr5:54302461..54302461hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135194
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5624800
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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