A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610652



Internal ID21558957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:491567..491567hg38UCSC Ensembl
chrY:402302..402302hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38747
hg19747
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170566
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610652
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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