A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5607682



Internal ID21555987
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 StatusM
Merged Variants
Supporting Variantsnssv17170145
SamplesNA19650
Known GenesPPP2R3B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5607682
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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