A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667332



Internal ID21615638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:648569..649464hg38UCSC Ensembl
chrY:559304..560199hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38896
hg19896
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17171024
SamplesHG00513
Known GenesSHOX
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667332
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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