A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170481



Internal ID21401335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:26393190..26393190hg38UCSC Ensembl
chrY:28539337..28539337hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5606991
Supporting Variants
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170481
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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