A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17171229



Internal ID21431768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:408505..408716hg38UCSC Ensembl
chrY:319240..319451hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5672339
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17171229
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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