A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615232



Internal ID21563537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:323555..323555hg38UCSC Ensembl
chrY:234290..234290hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38614
hg19614
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170672
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615232
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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