A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517060



Internal ID22575023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:13479445..13480966hg38UCSC Ensembl
chrY:15591325..15592846hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg381522
hg191522
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5969372
Supporting Variants
Samples
Known GenesUTY
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17517060
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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