A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169577



Internal ID21452929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:12085658..12087065hg38UCSC Ensembl
chrY:14206364..14207771hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg381408
hg191408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668792
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169577
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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