A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169945



Internal ID21403720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1681735..1681735hg38UCSC Ensembl
chrY:1750628..1750628hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38504
hg19504
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5608367
Supporting Variants
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169945
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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