A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170413



Internal ID21401544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:21539859..21553153hg38UCSC Ensembl
chrY:23701745..23715039hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3813295
hg1913295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665177
Supporting Variants
SamplesHG00096
Known GenesRBMY1A1, RBMY1B, RBMY1D
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170413
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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