A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17171219



Internal ID21415180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:406721..406989hg38UCSC Ensembl
chrY:317456..317724hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670276
Supporting Variants
SamplesHG00514
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17171219
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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