A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169647



Internal ID21512616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:15874263..15905518hg38UCSC Ensembl
chrY:17986143..18017398hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3831256
hg1931256
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665084
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169647
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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