A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169491



Internal ID21456007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:20060786..20295032hg38UCSC Ensembl
chrY:22222672..22456918hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38234247
hg19234247
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670878
Supporting Variants
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169491
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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