A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517062



Internal ID22575025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:13606591..13620703hg38UCSC Ensembl
chrY:15718471..15732583hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3814113
hg1914113
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970815
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17517062
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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