A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17359483



Internal ID22585152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13751202..13751258hg38UCSC Ensembl
chr10:13793202..13793258hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918444
Supporting Variants
Samples
Known GenesFRMD4A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17359483
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