A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666721



Internal ID21615028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:21049651..21067874hg38UCSC Ensembl
chrY:23211537..23229760hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3818224
hg1918224
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170403
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666721
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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