A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671232



Internal ID21619537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:12500482..12500649hg38UCSC Ensembl
chrY:14612276..14612443hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169205
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671232
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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