A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169224



Internal ID21479105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1284266..1284266hg38UCSC Ensembl
chrY:1353159..1353159hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5611563
Supporting Variants
SamplesHG03486
Known GenesCSF2RA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169224
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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