A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169849



Internal ID21464093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:17913558..17913614hg38UCSC Ensembl
chrY:20025438..20025494hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666618
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169849
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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