A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975856



Internal ID22750791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:19035816..19048763hg38UCSC Ensembl
chrY:21197702..21210649hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg3812948
hg1912948
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517095
Samples
Known GenesTTTY14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975856
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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