A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978949



Internal ID22753884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:19333766..19339287hg38UCSC Ensembl
chrY:21495652..21501173hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg385522
hg195522
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517099
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978949
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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