A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666813



Internal ID21615121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:489077..489492hg38UCSC Ensembl
chrY:399812..400227hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38416
hg19416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170564
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666813
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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