A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517095



Internal ID22575058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:19035816..19048763hg38UCSC Ensembl
chrY:21197702..21210649hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg3812948
hg1912948
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975856
Supporting Variants
Samples
Known GenesTTTY14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17517095
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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