A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437142



Internal ID22495012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22977420..22978266hg38UCSC Ensembl
chr7:23017039..23017885hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38847
hg19847
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5909411
Supporting Variants
Samples
Known GenesFAM126A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437142
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