A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5672490



Internal ID21620795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:26641473..26642566hg38UCSC Ensembl
chrY:28787620..28788713hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg381094
hg191094
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170500
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5672490
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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