A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517098



Internal ID22575061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:19280684..19283521hg38UCSC Ensembl
chrY:21442570..21445407hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg382838
hg192838
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5977767
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17517098
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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