A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169971



Internal ID21472769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:17560098..17560098hg38UCSC Ensembl
chrY:19671978..19671978hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5622926
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169971
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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