A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169835



Internal ID21473043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:17558230..17558230hg38UCSC Ensembl
chrY:19670110..19670110hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5609361
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169835
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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