A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170145



Internal ID21505818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:365930..365930hg38UCSC Ensembl
chrY:276665..276665hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg383962
hg193962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5607682
Supporting Variants
SamplesNA19650
Known GenesPPP2R3B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170145
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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