A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6073388



Internal ID21982621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:175871428..175871428hg38UCSC Ensembl
chr5:175298431..175298431hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572316
Samples
Known GenesCPLX2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6073388
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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