A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615355



Internal ID21563660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1270913..1270913hg38UCSC Ensembl
chrY:1339806..1339806hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169216
SamplesHG00512
Known GenesCSF2RA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615355
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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