A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367895



Internal ID22593564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48188701..48189497hg38UCSC Ensembl
chr10:49396744..49397540hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38797
hg19797
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5927527
Supporting Variants
Samples
Known GenesFRMPD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367895
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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