A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079602



Internal ID21988835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:137752181..137752181hg38UCSC Ensembl
chr5:137087870..137087870hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17540392
Samples
Known GenesHNRNPA0
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079602
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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