A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170490



Internal ID21504899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:26523252..26598567hg38UCSC Ensembl
chrY:28669399..28744714hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3875316
hg1975316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670633
Supporting Variants
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170490
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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