A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170547



Internal ID21505976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:347031..347140hg38UCSC Ensembl
chrY:257766..257875hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5667424
Supporting Variants
SamplesNA19983
Known GenesPPP2R3B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170547
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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