A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5604976



Internal ID21553281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:283654..283654hg38UCSC Ensembl
chrY:150321..150321hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170653
SamplesHG00513
Known GenesPLCXD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5604976
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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