A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170354



Internal ID21487594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:22712293..22712293hg38UCSC Ensembl
chrY:24858440..24858440hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5617235
Supporting Variants
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170354
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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