A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976288



Internal ID22751223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:8234352..8236951hg38UCSC Ensembl
chrY:8102393..8104992hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517419
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976288
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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