A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169474



Internal ID21487568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:14229269..14229269hg38UCSC Ensembl
chrY:16341149..16341149hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5607459
Supporting Variants
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169474
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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