A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169729



Internal ID21448110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11300434..11300532hg38UCSC Ensembl
chrY:13456110..13456208hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665248
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169729
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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