A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170148



Internal ID21457436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:368190..368263hg38UCSC Ensembl
chrY:278925..278998hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5664591
Supporting Variants
SamplesHG02587
Known GenesPPP2R3B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170148
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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