A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671113



Internal ID21619418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:268193..268577hg38UCSC Ensembl
chrY:134860..135244hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17171189
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671113
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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