A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970286



Internal ID22745221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:26587812..26627764hg38UCSC Ensembl
chrY:28733959..28773911hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3839953
hg1939953
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517363, nssv17517364
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970286
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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