A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169808



Internal ID21505881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1353160..1353228hg38UCSC Ensembl
chrY:1422053..1422121hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5671377
Supporting Variants
SamplesNA19983
Known GenesIL3RA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169808
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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