A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419724



Internal ID22477594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165098954..165099337hg38UCSC Ensembl
chr4:166020106..166020489hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5891754
Supporting Variants
Samples
Known GenesTMEM192
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419724
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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