A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5625931



Internal ID21574236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:172308909..172308909hg38UCSC Ensembl
chr5:171735913..171735913hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128905
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5625931
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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