A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969627



Internal ID22744562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:9800811..9816019hg38UCSC Ensembl
chrY:9638420..9653628hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3815209
hg1915209
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517430, nssv17517429
Samples
Known GenesTTTY22
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969627
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer