A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5607459



Internal ID21555764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:14229269..14229269hg38UCSC Ensembl
chrY:16341149..16341149hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169474
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5607459
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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