A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968606



Internal ID22743541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:15146910..15149552hg38UCSC Ensembl
chrY:17258790..17261432hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg382643
hg192643
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517076
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968606
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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