A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517055



Internal ID22575018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:12390193..12408233hg38UCSC Ensembl
chrY:14501988..14520032hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg3818041
hg1918045
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5976981
Supporting Variants
Samples
Known GenesGYG2P1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17517055
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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