A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17171220



Internal ID21506054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:406739..406739hg38UCSC Ensembl
chrY:317474..317474hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5622252
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17171220
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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