A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895914



Internal ID22671001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:9143882..9680194hg38UCSC Ensembl
chr4:9145608..9681818hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38536313
hg19536211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1558n209
Supporting Variantsnssv17415162
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)nsv5895914
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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