A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169219



Internal ID21507510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1278059..1278059hg38UCSC Ensembl
chrY:1346952..1346952hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5608577
Supporting Variants
SamplesNA19983
Known GenesCSF2RA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169219
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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