A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17495262



Internal ID22553195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:48652021..48661346hg38UCSC Ensembl
chr4:48654038..48663363hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg389326
hg199326
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5839052
Supporting Variants
Samples
Known GenesFRYL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17495262
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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