A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975974



Internal ID22750909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:12378991..12394505hg38UCSC Ensembl
chrY:14491215..14506300hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg3815515
hg1915086
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517053
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975974
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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