A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668834



Internal ID21617139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:9333077..9333196hg38UCSC Ensembl
chrY:9170686..9170805hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170944
SamplesHG00731
Known GenesTTTY20
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668834
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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