A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978655



Internal ID22753590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:15194070..15199721hg38UCSC Ensembl
chrY:17305950..17311601hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg385652
hg195652
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517077
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978655
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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