A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884854



Internal ID22659838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:14566697..14566799hg38UCSC Ensembl
chrY:16678577..16678679hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460858
Samples
Known GenesNLGN4Y
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884854
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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