A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17412560



Internal ID22470430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:133984608..134149257hg38UCSC Ensembl
chr4:134905763..135070412hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38164650
hg19164650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5902554
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17412560
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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