A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874707



Internal ID22649660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:26287753..26341246hg38UCSC Ensembl
chrY:28433900..28487393hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3853494
hg1953494
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453605
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874707
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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