A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170428



Internal ID21474611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:21669359..21669679hg38UCSC Ensembl
chrY:23831245..23831565hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5664826
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170428
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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