A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419660



Internal ID22477530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:9159413..9696820hg38UCSC Ensembl
chr4:9161139..9698444hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38537408
hg19537306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5906200
Supporting Variants
Samples
Known GenesDEFB131, MIR548I2, USP17L10, USP17L11, USP17L12, USP17L13, USP17L15, USP17L17, USP17L18, USP17L19, USP17L20, USP17L21, USP17L22, USP17L24, USP17L25, USP17L26, USP17L27, USP17L28, USP17L29, USP17L30, USP17L5, USP17L6P, USP17L9P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419660
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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