A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17453640



Internal ID22511514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:10227302..10243981hg38UCSC Ensembl
chrY:10064911..10081590hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3816680
hg1916680
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882434
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17453640
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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