A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967704



Internal ID22742639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:10176980..10179788hg38UCSC Ensembl
chrY:10014589..10017397hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg382809
hg192809
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517035
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967704
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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