A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169483



Internal ID21511073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1887490..1888077hg38UCSC Ensembl
chrY:1956383..1956970hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5671289
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169483
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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