A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980039



Internal ID22754974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:7384507..7417802hg38UCSC Ensembl
chrY:7252548..7285843hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3833296
hg1933296
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517412
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5980039
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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