A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565307



Internal ID20938378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:140299770..140300106hg38UCSC Ensembl
chr5:139679355..139679691hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267473
Samples
Known GenesPFDN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565307
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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