A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169503



Internal ID21510588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11379770..11379770hg38UCSC Ensembl
chrY:13535446..13535446hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5610075
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169503
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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