A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668732



Internal ID21617037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1884574..1884912hg38UCSC Ensembl
chrY:1953467..1953805hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169482
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668732
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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