A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517049



Internal ID22575012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:12252309..12264730hg38UCSC Ensembl
chrY:14373013..14385434hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg3812422
hg1912422
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5980126
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17517049
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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