A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169803



Internal ID21414946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1340097..1340188hg38UCSC Ensembl
chrY:1408990..1409081hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665334
Supporting Variants
SamplesHG00513
Known GenesIL3RA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169803
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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