A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666976



Internal ID21615282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11391302..11393909hg38UCSC Ensembl
chrY:13546978..13549585hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg382608
hg192608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169505
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666976
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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