A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5605866



Internal ID21554171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1314566..1314566hg38UCSC Ensembl
chrY:1383459..1383459hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38247
hg19247
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169787
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5605866
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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