A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5629079



Internal ID21577384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:92435543..92435543hg38UCSC Ensembl
chr5:91771250..91771250hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17139900
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5629079
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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