A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17495549



Internal ID22553482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138306586..138313251hg38UCSC Ensembl
chr5:137642275..137648940hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg386666
hg196666
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5841145
Supporting Variants
Samples
Known GenesCDC25C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17495549
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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