A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5618842



Internal ID21567147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:23995173..23995173hg38UCSC Ensembl
chrY:26141320..26141320hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38639
hg19639
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17171180
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5618842
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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