A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169208



Internal ID21474161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1253324..1253324hg38UCSC Ensembl
chrY:1322217..1322217hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5619858
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169208
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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