A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437283



Internal ID22495153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:35584272..35584397hg38UCSC Ensembl
chr8:35441790..35441915hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5908558
Supporting Variants
Samples
Known GenesUNC5D
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437283
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