A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17171192



Internal ID21477814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:268291..268291hg38UCSC Ensembl
chrY:134958..134958hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg387097
hg197097
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5607239
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17171192
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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