A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170412



Internal ID21483573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:21453864..21453864hg38UCSC Ensembl
chrY:23615750..23615750hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604787
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170412
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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