A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17499658



Internal ID22557594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:146640539..146672116hg38UCSC Ensembl
chr4:147561691..147593268hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg3831578
hg1931578
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5838051
Supporting Variants
Samples
Known GenesPOU4F2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17499658
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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