A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17171332



Internal ID21464517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:9847846..9847926hg38UCSC Ensembl
chrY:9685455..9685535hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665202
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17171332
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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