A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5622732



Internal ID21571037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1278309..1278309hg38UCSC Ensembl
chrY:1347202..1347202hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169220
SamplesHG00512
Known GenesCSF2RA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5622732
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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