A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970399



Internal ID22745334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:10188023..10196137hg38UCSC Ensembl
chrY:10025632..10033746hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg388115
hg198115
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517036
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970399
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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