A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979209



Internal ID22754144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:21194546..21196819hg38UCSC Ensembl
chrY:23356432..23358705hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg382274
hg192274
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517316
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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