A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878244



Internal ID22653209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11826830..11963694hg38UCSC Ensembl
chrY:13947536..14084400hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg38136865
hg19136865
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465682
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878244
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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