A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884221



Internal ID22659203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:20486601..20486673hg38UCSC Ensembl
chrY:22648487..22648559hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464467
Samples
Known GenesTTTY10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884221
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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