A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17494484



Internal ID22552415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38407314..38409710hg38UCSC Ensembl
chr4:38408935..38411331hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382397
hg192397
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5839568
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17494484
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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