A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5604672



Internal ID21520359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:323810..323810hg38UCSC Ensembl
chrY:234545..234545hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg385120
hg195120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170677, nssv17170678, nssv17170679
SamplesHG00512, NA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5604672
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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