A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5614886



Internal ID21563191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:26402906..26402906hg38UCSC Ensembl
chrY:28549053..28549053hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170482
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5614886
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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