A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671934



Internal ID21620241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:9361810..9552074hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38190265
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170945
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671934
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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