A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882026



Internal ID22657003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:10204952..10205476hg38UCSC Ensembl
chrY:10042561..10043085hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38525
hg19525
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454910
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882026
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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