A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665690



Internal ID21613995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:10002..47580hg38UCSC Ensembl
chr4:10002..47576hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3837579
hg1937575
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17127309
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665690
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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