A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5672339



Internal ID21620644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:408505..408716hg38UCSC Ensembl
chrY:319240..319451hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17171229
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5672339
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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