A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17171301



Internal ID21473963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:57215630..57215630hg38UCSC Ensembl
chrY:59361781..59361781hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605864
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17171301
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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