A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868151



Internal ID22643086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11134270..11134377hg38UCSC Ensembl
chrY:13289946..13290053hg19UCSC Ensembl
CytobandYq11.1
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458761
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868151
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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