A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5619034



Internal ID21567339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:25266767..25266767hg38UCSC Ensembl
chrY:27412914..27412914hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169937
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5619034
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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