A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170756



Internal ID21501181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:56676100..56677244hg38UCSC Ensembl
chrY:58913627..58914771hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg381145
hg191145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5667139
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170756
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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