A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5672166



Internal ID21620471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:6075940..6076268hg38UCSC Ensembl
chrY:5943981..5944309hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170777
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5672166
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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