A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871567



Internal ID22646505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:13789207..14020093hg38UCSC Ensembl
chrY:15901087..16131973hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg38230887
hg19230887
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466851
Samples
Known GenesVCY, VCY1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871567
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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