A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170651



Internal ID21414659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:280962..280962hg38UCSC Ensembl
chrY:147629..147629hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38422
hg19422
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5615374
Supporting Variants
SamplesHG00513
Known GenesPLCXD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170651
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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