A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517061



Internal ID22575024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:13584001..13585841hg38UCSC Ensembl
chrY:15695881..15697721hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg381841
hg191841
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5974738
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17517061
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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