A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170514



Internal ID21431554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:26652805..26652805hg38UCSC Ensembl
chrY:28798952..28798952hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5607775
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170514
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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