A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17368929



Internal ID22594598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125505372..125505871hg38UCSC Ensembl
chr11:125375268..125375767hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5923784
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17368929
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