A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170149



Internal ID21431421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:368326..368474hg38UCSC Ensembl
chrY:279061..279209hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5672202
Supporting Variants
SamplesHG00731
Known GenesPPP2R3B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170149
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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