A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517099



Internal ID22575062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:19333766..19339287hg38UCSC Ensembl
chrY:21495652..21501173hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg385522
hg195522
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5978949
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17517099
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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