A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5625110



Internal ID21573415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:174870840..174870840hg38UCSC Ensembl
chr5:174297843..174297843hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38208
hg19208
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17139144
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5625110
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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