A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517103



Internal ID22575066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:20047380..20050122hg38UCSC Ensembl
chrY:22209266..22212008hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg382743
hg192743
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5974299
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17517103
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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