A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669041



Internal ID21617346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:56690486..56690776hg38UCSC Ensembl
chrY:58900095..58900385hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170993
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669041
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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