A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17363684



Internal ID22589353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13742054..13742895hg38UCSC Ensembl
chr10:13784054..13784895hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38842
hg19842
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5921352
Supporting Variants
Samples
Known GenesFRMD4A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17363684
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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