A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17492297



Internal ID22550224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10262087..10266077hg38UCSC Ensembl
chr5:10262199..10266189hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg383991
hg193991
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5840288
Supporting Variants
Samples
Known GenesCCT5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17492297
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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