A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17418658



Internal ID22476528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155194161..155194285hg38UCSC Ensembl
chr4:156115313..156115437hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5893811
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17418658
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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